Prescription Drug Program Prior Authorization Criteria

Prescription Drug Program Prior Authorization Criteria
Revised 2/03/2015
This document is an informational listing of the medications requiring a Prior Authorization through the Arkansas Medicaid
Pharmacy Program, and a description of the associated criteria. Inclusion in this document does not guarantee market
availability and products must meet the Centers for Medicare and Medicaid Services (CMS) definition of a covered
outpatient drug and pay CMS rebate to be covered by Arkansas Medicaid. Select covered over the counter medications
are covered pursuant to a valid prescription, but are not covered for Long Term Care eligible beneficiaries.
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Prescription Product or Drug Class
5-HT3 or NK1 Receptor Antagonists
Abiraterone Acetate Tablet (Zytiga)
Acetic Acid HC Ear Drops
Acitretin Capsule (Soriatane)
Aclidinium Bromide Inhaler (Tudorza Pressair)
Acthar HP Gel Injection
Actonel
Acyclovir (Xerese and Zovirax Cream)
Acyclovir Orally Disintegrating Delayed Release Tablet (Sitavig)
Adempas (Riociguat) Tablet
Adoxa
Afatinib Dimaleate Tablet (Gilotrif)
Afinitor
Alagesic Liquid Oral Solution 50-325-40/15ml
Albuterol Oral Tablets and Syrup
Aldara
Allergan Extracts
Altabax 1% Ointment
Amitiza
Ampyra ER
Angiotensin II Receptor Antagonists
Anoro Ellipta
Antibiotic Ophthalmic Drops (Moxeza,Vigamox, Quixin, Iquix, Azasite, Zymar)
Antibiotic-Steroid Fixed-Dose Combination Ophthalmic Drops (Cortisporin,
Tobradex ST, Zylet)
Antibiotics, Long-acting
Antidepressant, Second Generation (SGAD)
Antidiabetic Agents
Anti-Inflammatory Ophthalmic Drops
Anti-Inflammatory Agents, Nonsteroidal
Antihistamine Eye Drops, Mast Cell Stabilizers, and Combination Mast Cell
Stabilizer-Antihistamine Eye Drops
Antihistamines, Second Generation
Antifungal Creams (Topical), Lotions, and Shampoos
Antipsychotics, Injectable Long-acting
Antipsychotics, Oral
Aptiom
Aranesp
Armodafinil (Nuvigil)
Aromatase Inhibitors (Femara Tablets and Arimidex)
Astragraf XL
Attention Deficit (ADD/ADHD) Agents for Children (Age Less than 18 Years)
Attention Deficit (ADD/ADHD) Agents for Adults (Age 18 Years or greater)
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Auranolfin (Ridaura)
Axitinib Tablet (Inlyta)
Azelaic Acid 15% Gel (Finacea)
Azithromycin (Azithromycin Powder Packets and ZMAX Suspension)
Aztreonam Inhalation Solution (Cayston)
Baraclude
Becaplermin (Regranex)
Bedaquiline Fumarate (Sirturo)
Belimumab (Benlysta)
Benign Prostatic Hypertrophy (BPH) Drugs
Benzodiazepine Solid Oral Dosage Forms
Benzodiazepine Liquid Oral Dosage Forms
Benzoic Acid 6%, Salicyclic Acid 3%, Oak Bark Extract (Bensal HP) Ointment
Beta Adrenergic Blocking Agents
Beta2 Agonists/Corticosteroids, Inhaled
Bethkis
Bexarotene Gel (Targretin)
BiDil
Binosto
Boniva
Bosutinib (Bosulif)
Botox
Bowel Prep Kits
Bronchodilators, Long-Acting
Bronchodilators, Short-Acting
Budesonide EC Capsule (Entocort EC)
Buprenorphine (Subutex)
Buprenorphine-Naloxone (Suboxone)
Buproprion (Zyban)
Butalbital Products
C1 Esterase inhibitor (Cinryze)
CII Stimulants
Calcipotriene Cream, Foam, Ointment, or Scalp Solution (Dovonex, Sorilux)
Calcipotriene and Betamethasone Dipropionate Ointment (Taclonex)
Calcitonin-Salmon Nasal Spray (Miacalcin or Fortical)
Calcitonin-Salmon Injection (Miacalcin)
Calcitriol (Vectical)
Calcium Channel Blockers
Carbidopa (Lodosyn)
Carbidopa/Levodopa/Entacapone (Stalevo)
Cephalexin 750mg Capsule (Keflex)
Cephalosporins – 3rd Generation
Ceritinib (Zykadia)
Chlorpheniramine ER 12mg
Ciclopirox 8% Kit
Cidofovir (Vistide)
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Cinryze
Ciprofloxacin Extended-Release (Cipro XR)
Clobazam (Onfi)
Clonazepam Oral Disintegrating Tablet
Clonidine
Clonidine Vials
Colchicine 0.6mg Tablets (Colcrys)
Cometriq
COPD Agents
Corticosteroids, Nasal Inhaled
Corticosteroids, Oral Inhaled
Corticosteroids, Topical
Crizotinib (Xalkori)
Cromolyn Sodium Oral Solution (Gastrocrom)
Crotamiton Cream and Lotion (Eurax)
Cuprimine
Cyclosporine 0.05% Eye Emulsion (Restasis)
Cyproheptadine 4mg/10ml U.D. Cup
Cysteamine Opthalmic Drops (Cystaran)
Cysteamine DR Oral Capsule (Procysbi)
Dabigatran Etexilate Mesylate (Pradaxa)
Dabrafenib (Tafinlar)
Dalfampridine ER (Ampyra ER)
Daliresp
Dasatinib (Sprycel) Tablet
Deferiprone (Ferriprox) Tablet
Denosumab (Prolia)
Depen
Desmopressin Nasal Spray/Solution (DDAVP)
Dexamethasone Dose Pack (Dexpak and Zema-Pak)
Dextromethorphan Hbr/Quinidine Capsule (Nuedexta)
Diclegis DR 10-10
Dihydroergotamine Mesylate Nasal Spray (Migranal)
Direct Renin Inhibitors
Disopyramide CR (Norpace CR)
Dornase Alfa Inhalation Solution (Pulmozyme)
Doryx
Dorzolamide-Timolol 2%-0.5% PF (Cosopt PF)
Doxepin 5% Cream (Prudoxin, Zonalon)
Doxycycline
Doxylamine Succinate 5mg Chewable Tablet (Aldex AN)
Doxylamine Succinate 10mg and Pyridoxine 10mg (Diclegis DR 10-10)
Dronabinol (Marinol)
Droxidopa (Northera) Capsule
Efinaconazole 10% Solution (Jublia)
Eliglustat (Cerdelga)
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Eliquis
Emtricitabine (Emtriva)
Entacapone (Comtan)
Enzalutamide (Xtandi)
Eslicarbazepine (Aptiom)
Etanercept (Enbrel)
Entecavir (Baraclude)
Entocort EC
Epogen
Erythropoiesis Stimulating Agents
Estrogen Replacement Agents
Everolimus (Afinitor)
Exelon
Famotidine Oral Suspension (Pepcid)
Febuxostat Tablet (Uloric)
Fenofibrate and Fenobibric Acid Products
Fentanyl Buccal Tablet (Fentora and Onsolis)
Fentanyl Nasal Spray (Lazanda)
Fentanyl Citrate Sublingual (Abstral)
Fentanyl Citrate Sublingual Spray (Subsys)
Fentanyl Citrate Oral Transmucosal (Actiq)
Fibromyalgia Agents
Fidaxomicin (Dificid)
Finasteride Tablet (Proscar)
Flagyl ER
Fluorouracil 0.5% Cream (Carac)
Fluorouracil 1% Cream (Fluoroplex)
Fluorouracil 2% and 5% Solution (Efudex)
Fluorouracil 5% Cream (Efudex)
Fosamax Oral Solution
Fosamax Plus D
Fosamprenavir (Lexiva) Tablet
Fosamprenavir (Lexiva) Suspension
Forteo
Fulyzaq
Galantamine ER (Razadyne ER)
Galantamine Solution (Razadyne)
Gattex
Giazo
Glycerol Phenylbutyrate Oral Liquid (Ravicti)
Glycophos
Glycopyrrolate 0.2mg/ml vial
Glycopyrrolate 1.5mg Tablet (Glycate)
Guanfacine
Hemorrhoid Preparations
Hepatitis C Virus Medications
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
HMG-CoA Reductase Inhibitors
Hydrocodone ER (Zohydro ER) Capsule
Hydroxypropyl 5mg Eye Insert (Lacrisert)
Ibrutinib (Imbruvica) Capsule
Icatibant Syringe (Firazyr)
Iclusig
Idelalisib (Zydelig) Tablet
Imiquimod (Aldara)
Imiquimod (Zyclara)
Immunologic Agents (Multiple Sclerosis)
Infergen
Ingenol Mebutate (Picato Gel)
Inhaled Corticosteroid (ICS)/Long-Acting Beta Agonist (LABA) Combination
Products
Insulin Pens
Isosorbide Dinitrate/Hydralazine HCl (BiDil)
Isotretinoin (Accutane)
Itraconazle 200mg Tablet (Onmel)
Itraconazole Oral Solution (Sporanox)
Ivacaftor Tablet (Kalydeco)
Ivermectin 0.5% Lotion (Sklice)
Juxtapid
Keppra ER
Ketorolac (Toradol)
Kits
Korlym
Kynamro
Lamotrigine Start Kits (Lamictal Start Kits)
Lansoprazole, Amoxicillin, and Clarithromycin Combination (Prevpac)
Leukotriene Receptor Antagonists
Levetiracetam ER (Keppra ER)
Levofloxacin 500mg/20ml U.D. Cup
Levothyroxine Capsule (Tirosint)
Levothyroxine Vial
Lexiva Oral Suspension
Lexiva Tablets
Lidocaine 5% Patch (Lidoderm)
Lidocaine-Prilocaine2.5%-2.5% Topical Cream (Emla)
Linacoltide (Linzess)
Lithium ER
Lithobid SA
Lindane
Lovaza
Low Molecular Weight Heparins
Lubiprostone (Amitiza)
Lupaneta
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Lupron
Malathion (Ovide)
Macitentan (Opsumit)
Marinol
Maraviroc (Selzentry)
Mecamylamine HCL Tablet (Vecamyl)
Mechlorethamine HCL Gel (Valchlor)
Medroxyprogesterone (Depo-Provera)
Megestrol (Megace and Megace ES)
Mekinist
Memantine XR (Namenda XR)
Memantine Solution (Namenda)
Meprobamate (Equanil) Tablet
Mepron
Mercaptopurine (Purixan)
Mesalamine 1000mg (Canasa)
Mestinon Timespan
Methoxsalen (Oxsoralen-Ultra, 8-MOP)
Metreleptin Vial (Myalept)
Metformin Oral Solution(Riomet)
Metformin ER (Fortamet ER and Glumetza ER)
Methscopolamine (Pamine, Pamine Forte, Pamine FQ)
Methotrexate Auto Inj. (Otrexup)
Methotrexate (Trexall)
Methylnaltrexone Bromide (Relistor) SQ Injection
Metozolv
Metronidazole 1% Cream (Noritate)
Metronidazole 1% Gel (Metrogel)
Metronidazole 375mg (Flagyl)
Metronidazole ER 750mg (Flagyl)
Metronidazole/Tetracycline/Bismuth (Helidac and Pylera)
Miconazole 50mg Buccal Tablet (Oravig)
Miconazole Nitrate/ Zinc Oxide/White Petrolatum (Vusion)
Mifepristone (Korlym)
Mig Lustat (Zavesca)
Migranal Nasal Spray
Millipred
Minocycline
Mirapex ER
Misoprostol (Cytotec)
Modafinil (Provigil)
Moxatag
Multiple Sclerosis Agents
Mycophenolate (Cellcept, Myfortic)
Nabilone (Cesamet)
Nafarelin Nasal Spray (Synarel)
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Naloxone Auto-injector (Evzio)
Namenda
Namenda XR
Nandrolone Decanoate Injection
Neuropathic Pain Agents
Nevirapine XR (Viramune XR)
Nevirapine Oral Suspension (Viramune)
Nicotine Replacement Therapy
Nimodipine Solution (Nymalize)
Nitisinone (Orfadin)
Nitrofurantoin Suspension (Furadantin)
Nitroglycerin 0.4% Rectal Ointment (Rective)
Nizatadine Oral Solution (Axid)
Non-Benzodiazepine Sedative Hypnotics
Nonsteroidal Anti-Inflammatory Agents
Norpace CR
Noxafil Suspension
Noxafil DR Tablet
Noxafil Vial
Nucort
Nuzon Gel
Omega-3-acid ethyl esters (Lovaza)
Omeprazole/Clarithromycin/Amoxicillin (Omeclamox-Pak)
Onabotulinumtoxina (Botox 200 Units)
Onfi
Opioids, Long-Acting
Opioids, Short-Acting
Opium Tinture
Opsumit (Macitentan)
Oracea
Orapred ODT Tablets
Oseltamivir Suspension (Tamiflu Suspension)
Osteoporosis Drugs
Otic Preparations
Otrexup
Overactive Bladder Agents
Oxandrolone (Oxandrin)
Oxymethalone (Anadrol-50)
Pain Medications, Injectable
Papaverine Injection
Pasireotide Diaspartate (Signifor)
Pazopanib (Votrient)
Peg Intron
Pegasys
PegInterferon Alfa-2B (Sylatron)
Pegvisomant Injection (Somavert)
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Penciclovir (Denavir)
Penicillamine (Depen 250mg Tablet and Cuprimine 250mg Capsule)
Perampanel Tablet (Fycompa)
Phosphate Removing Agents
Pimecrolimus (Elidel)
Podofilox (Condylox 0.5% Topical Solution/Gel)
Pomalyst
Posaconazole (Noxafil)
Potassium Chloride Capsule and Packet
Pradaxa
Pramipexole ER (Mirapex ER)
Prednisolone
Prednisone (Rayos DR)
Procrit
Procysbi
Prolia
Promacta
Propafenone SR (Rythmol SR)
Proquin
Proton Pump Inhibitors
Pyridostigmine Timespan (Mestinon Timespan)
Quick Relief Medications for Asthma
Quinine Sulfate (Qualaquin)
Raloxifene (Evista)
Ranolazine (Ranexa)
Razadyne ER
Razadyne Solution
Rebetol
Ravicti
Regorafenib (Stivarga)
Requip XL
Respiratory Syncytial Virus (RSV) Medications
Restasis
Ribapak
Ribasphere
Ribavirin
Ridaura
Rifaximin Tablet (Xifaxan)
Rilonacept Sub-Q Vial (Arcalyst)
Riociguat (Adempas) Tablet
Rivaroxaban10mg Tablet (Xarelto)
Rivaroxaban 15mg and 20mg Tablet (Xarelto)
Rivastigmine Soution (Exelon) Solution
Ropinirole XL (Requip XL)
Rosacea Treatment
Rotigotine (Neupro) Patch
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Ruxolitinib (Jakafi)
Rythmol SR
Sapropterin HCL (Kuvan)
Scopolamine Transermal Patch
Sedative Hypnotics
Serostim
Serotonin 5-HT1 Receptor Agonists
Signifor
Sildenafil (Revatio)
Siltuximab Vial (Sylvant)
Sinecatechins (Veregen Ointment 15%)
Skeletal Muscle Relaxants
Sodium Chloride 7% Inhalation Solution (Hyper-Sal 7%)
Sodium Oxybate (Xyrem)
Somatropin (Genotropin)
Somatropin (Humatrope)
Somatropin (Norditropin)
Somatropin (Nutropin)
Somatropin (Omnitrope)
Somatropin (Saizen)
Somatropin (Tev-tropin)
Somatropin (Zorbtive)
Soriatane
Spinosad 0.9% Topical Suspension (Natroba)
Spiriva
Suboxone
Subutex
Sucralfate Suspension (Carafate)
Sulfamethoxazole-Trimethoprim U.D. Cup
Sunitinib (Sutent)
Symbicort
Synagis
Syprine
Tacrolimus (Astagraf XL)
Tacrolimus (Protopic)
Tadalafil (Adcirca)
Tafinlar
Tamiflu Suspension
Tamoxifen Solution (Soltamox)
Targeted Immune Modulators
Targretin
Tasimelteon (Hetlioz)
Tavaborole (Kerydin)
Tazarotene Gel/Cream (Tazorac)
Tedizolid (Sivextro)
Telithromycin (Ketek)
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Temazepam 7.5mg and 22.5mg Capsule (Restoril)
Tenofovir (Viread)
Tenofovir/Emtricitabine (Truvada)
Terbinafine (Lamisil)
Terbinex
Teriparatide (Forteo)
Testosterone Replacement Products
Tetrabenazine (Xenazine)
Timolol Maleate/Dorzolamide HCL (Cosopt PF)
Tiotropium Bormide Inhaler (Spiriva)
Tirosint
Tobacco Cessation Products
Tobramycin Inhalation Solution (TOBI - Brand)
Tobramycin Inhalation Solution (Generic) (Bethkis)
Tobramycin Inhalation Powder (TOBI Podhaler)
Topical Corticosteroids
Topical Products
Topiramate XL (Qudexy XL or Trokendi XL)
Tramadol ER
Tramadol IR
Tramadol-Acetaminophen (Ultracet)
Trametinib (Mekinist)
Tranexamic Acid (Lysteda)
Transdermal Scopolamine Patch
Trazodone (Trazodone 300mg, Oleptro ER)
Trexall
Trientine HCl (Syprine)
Tudorza Pressair Inhaler
Ulesfia
Uloric
Valchlor
Valcyte Solution
Varenicline (Chantix)
Vascepa
Vecamyl
Vemurafenib (Zelboraf)
Veregen
Veripred Solution
Viramune XR
Viramune Oral Suspension
Vismodegib Capsule (Erivedge)
Vorapaxar (Zontivity)
Votrient
Xarelto 10mg, 15mg & 20mg, Starter Pack
Xgeva
Xyrem
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Xolair
Zohyrdro ER
Appendix A – Nil per os (NPO)
Appendix B – Approved Tracheostomy Codes
Appendix C – Topical Corticosteroids, No PA Required
Appendix D – Congestive Heart Failure Diagnoses
Appendix E – Malignant Cancer Diagnoses
Appendix F – Antineoplastics to Infer Malignant Cancer
Appendix G – Chronic Obstruction Pulmonary Disease Diagnoses
Appendix H – Approved Diagnoses for nonpreferred Antiepileptic Agents in
Neuropathic Pain Agent Class
Appendix I – Approved Endoscopy Code
Prescribers may request an override for nonpreferred drugs by calling the
UAMS College of Pharmacy Evidence-Based Prescription Drug Program
Help Desk at 1-866-250-2518 (toll-free) or 501-526-4200 (local.) The
Arkansas Medicaid Preferred Drug List may be found at this link.
https://www.medicaid.state.ar.us/Download/provider/pharm/PDL.xls
For assistance on all other drugs, prescribers may call the HP Pharmacy
Unit at 1-800-707-3854 (toll-free) or 501-374-6609 x500 (local.) The
appropriate number is indicated with the associated drug.
Please refer to the Arkansas Medicaid Webpage at www.medicaid.state.ar.us
for a complete list of drugs.
Other claim edits for age, gender, quantity, dose and/or cumulative quantity
may apply.
https://www.medicaid.state.ar.us/Download/provider/pharm/ClaimEdits.xls
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
5-HT3 or NK1 Receptor Antagonists
(Implemented 09/14/2009)
Prescribers may request an override for nonpreferred drugs by calling the
UAMS College of Pharmacy Evidence-Based Prescription Drug Program
Help Desk at 1-866-250-2518 (toll-free) or 501-526-4200 (local).
Preferred agents with criteria




Ondansetron HCl 4mg, 8mg tablet (Zofran)
Ondansetron 4mg, 8mg oral-disintegrating tablet (Zofran ODT)
Ondansetron 4mg/2ml preservative-free vial (Zofran)
Ondansetron 40mg/20ml vial (Zofran)
Nonpreferred agents

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
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

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Aprepitant (Emend)
Dolasetron (Anzemet)
Granisetron (Kytril, Sancuso)
Netupitant-Palonosetron HCl (Akynzeo)
Ondansetron 24mg tablet (Zofran)
Ondansetron 32mg/50ml bag (Zofran)
Ondansetron 4mg/2ml ampule and syringe (Zofran)
Ondansetron 4mg/5ml solution (Zofran)
Ondansetron Soluble Film (Zuplenz)
Approval criteria for preferred agents with criteria
No therapeutic duplication with other 5-HT3 receptor antagonists
Additional criteria
Quantity limits apply
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Abiraterone AcetateTablet (Zytiga)
(Implemented 12/10/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Zytiga
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Acitretin Capsule (Soriatane)
(Implemented 03/26/2008)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Soriatane
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Aclidinium Bromide Inhaler (Tudorza Pressair)
(Implemented 12/19/2012)
Prescribers may request an override for nonpreferred drugs by calling the
UAMS College of Pharmacy Evidence-Based Prescription Drug Program
Help Desk at 1-866-250-2518 (toll-free) or 501-526-4200 (local).
Approval criteria



Diagnosis of COPD in Medicaid history in previous 2 years; AND
No therapeutic duplication with overlapping days’ supply between
Anoro Ellipta, Spiriva, and/or Tudorza; AND
Medicaid recipient is > 18 years of age; AND
Denial criteria


Lack of approval criteria; OR
Diagnosis of asthma in Medicaid history in previous 2 years
Additional criteria

Quantity edits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Acyclovir Cream, Ointment
(Implemented 03/19/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that do not require prior authorization

Docosanol 10% (Abreva) cream
Drugs that require manual review for prior authorization




Acyclovir (Zovirax) 5% cream
Acyclovir (Zovirax) 5% ointment
Acyclovir-Hydrocortisone (Xerese) 5%-1% cream
Penciclovir (Denavir) 1% cream 5 gram (Implemented 09/23/2014)
Additional criteria

Quantity edits apply
Link to Memorandum
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Acyclovir Orally Disintegrating Delayed Release Tablet
(Sitavig)
(Implemented 09/23/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Sitavig
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Afatinib Dimaleate Tablet (Gilotrif)
(Implemented 12/10/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Gilotrif
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Alagesic Liquid Oral Solution 50-325-40/15ml
(Implemented 01/18/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria

NPO (Appendix A)
Age Edit

Recipients must be 12 years of age or greater
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Albuterol Oral Tablets and Syrup
(Implemented 03/18/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization





Albuterol 2mg/5ml Syrup
Albuterol 4mg ER
Vospire 4mg ER
Albuterol 8mg ER
Vospire 8mg ER
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Allergan Extracts, (short Ragweed Pollen Allergan
Extract) and (Timothy Grass Pollen Allergen Extract)
(Implemented 09/23/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization


Ragwitek
Grastek
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Angiotensin II Receptor Antagonists
(Implemented 10/01/2008)
Prescribers may request an override for nonpreferred drugs by calling the
UAMS College of Pharmacy Evidence-Based Prescription Drug Program
Help Desk at 1-866-250-2518 (toll-free) or 501-526-4200 (local).
Preferred agents with criteria


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


Diovan (Brand only)
Irbesartan (Avapro)
Irbesartan/HCTZ (Avalide)
Losartan potassium (Cozaar)
Losartan potassium/HCTZ (Hyzaar)
Olmesartan medoxomil (Benicar)
Olmesartan medoxomil/Amlodipine besylate (Azor)
Olmesartan medoxomil/Amlodipine besylate/HCTZ (Tribenzor)
Olmesartan medoxomil/HCTZ (Benicar HCT)
Valsartan/Amlodipine (Exforge)
Valsartan/Amlodipine/HCTZ (Exforge HCT)
Valsartan/HCTZ (Diovan HCT)
Nonpreferred agents
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
Azilsartan medoxomil (Edarbi)
Azilsartan medoxomil/Chlorthalidone (Edarbyclor)
Candesartan cilexetil/HCTZ (Atacand HCT)
Eprosartan mesylate (Teveten)
Eprosartan mesylate/HCTZ (Teveten HCT)
Telmisartan (Micardis)
Telmisartan/Amlodipine (Twynsta)
Telmisartan/HCTZ (Micardis HCT)
Valsartan (generic Diovan)
Approval criteria for preferred agent with criteria
New Starts will require a paid claim in history of an ACE-Inhibitor product (ACEInhibitor, ACE-Inhibitor/HCTZ, or ACE-Inhibitor/Calcium Channel Blocker) in the
previous 27-45 days
OR
Continuation of therapy will require at least one paid claim in history of a
“Preferred with criteria” angiotensin receptor blocker or direct renin inhibitor in the
past 60 days
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Nonpreferred agent with criteria
Candesartan cilexetil (Atacand)
Approval criteria for nonpreferred agent with criteria
Candesartan cilexetil (Atacand)
 Congestive heart failure (Appendix D)
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Antibiotic Ophthalmic Drops
(Implemented 08/21/2009)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
History of at least two claims for two different products that do not require prior
authorization within the previous 30 days
Gentamicin 3mg/ml eye drops, Sulfacetamide 10% eye drops, and Tobramycin
0.3% eye drops are available agents that do not require PA but are not included
in this approval criteria.
ANTIBIOTIC OPHTHALMIC DROPS
GENERIC NAME
COMMON TRADE NAME*
PA STATUS
Ciprofloxacin 0.3% eye drops
Ciloxan® 0.3% eye drops
No PA
Neomycin-Polymyxin B-Gramicidin eye drops
Neosporin® eye drops
No PA
Ofloxacin 0.3% eye drops
Ocuflox® 0.3% eye drops
No PA
GENERIC NAME
COMMON TRADE NAME*
PA STATUS
Azithromycin 1% eye drops
Azasite® 1% eye drops
PA
Besifloxacin HCl 0.6% eye drops
Besivance® 0.6% eye drops
PA
Gatifloxacin 0.5% eye drops
Zymaxid® 0.5% eye drops
PA
Levofloxacin 0.5% eye drops
Quixin® 0.5% eye drops
PA
Moxifloxacin 0.5% eye drops
Moxeza® 0.5% eye drops
PA
Moxifloxacin HCl 0.5% eye drops
Vigamox® 0.5% eye drops
PA
*TRADE NAMES ARE FOR REFERENCE ONLY
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Antibiotic-Steroid Fixed-Dose Combination Opthalmic
Drops (Cortisporin, Tobradex ST, Zylet)
(Implemented 10/11/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria

History of at least two claims for two different products that do not require
prior authorization within the previous 31 days
o One claim must have been in the previous 14-31 days, AND
o One claim must have been in the previous 5-13 days.
ANTIBIOTIC OPHTHALMIC DROPS
GENERIC NAME
COMMON TRADE NAME*
PA STATUS
Gentamicin-Prednisolone eye drops
Pred-G® 1% eye drops
No PA
Neomycin-Polymyxin B-Dexamethasone eye drops
Maxitrol® eye drops
No PA
Sodium Sulfacetamide-Prednisolone eye drops
Blephamide® eye drops
No PA
Sodium Sulfacetamide-Prednisolone eye drops
Sulf-Pred® 10-0.23% eye drops
No PA
Tobramycin/Dexamethasone eye drops
Tobradex® eye drops
No PA
GENERIC NAME
COMMON TRADE NAME*
PA STATUS
Neomycin-Polymyxin B-Hydrocortisone eye drops
Cortisporin® eye drops
PA
Tobramycin-Dexamethasone eye drops
Tobradex ST® eye drops
PA
Tobramycin-Loteprednol eye drops
Zylet® eye drops
PA
*TRADE NAMES ARE FOR REFERENCE ONLY
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Antibiotics, Long-acting
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
(Implemented 09/21/2009 and 8/17/2010)
Drugs that do not require prior authorization
Generic MAC’d short-acting antibiotics are available without a prior authorization.
Drugs that require manual review for prior authorization



Amoxicillin ER 775mg (Moxatag ER)
Ciprofloxacin ER 500mg, 1000mg (Cipro XR, Proquin XR)
Metronidazole ER 750mg (Flagyl ER)
Link to Memorandum: Clarithromycin XL, Flagyl ER 750 mg
Link to Memorandum: Removal of manual review for Clarithromycin XL
Link to Memorandum: Ciprofloxacin ER, Proquin, Moxatag
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Second-generation Antidepressants (SGAD)
(Implemented 01/01/2010)
Prescribers may request an override for nonpreferred drugs by calling the
UAMS College of Pharmacy Evidence-Based Prescription Drug Program
Help Desk at 1-866-250-2518 (toll-free) or 501-526-4200 (local).
Preferred agents with criteria












Bupropion HCl regular-release (Wellbutrin)
Bupropion HCl extended-release (Wellbutrin XL)
Bupropion HCl sustained-release (Wellbutrin SR)
Citalopram hydrobromide (Celexa)
Escitalopram oxalate (Lexapro)
Fluoxetine HCl 10mg, 20mg capsule, and 20mg/5ml solution (Prozac)
Fluvoxamine maleate (Luvox)
Mirtazapine 15mg, 30mg, 45mg tablet (Remeron)
Paroxetine HCl regular-release tablet (Paxil)
Sertraline HCl (Zoloft)
Venlafaxine HCl extended-release capsule (Effexor ER)
Venlafaxine HCl regular-release tablet (Effexor)
Nonpreferred agents with SGAD criteria















Bupropion hydrobromide extended-release tablet (Aplenzin)
Bupropion HCl exended-release tablet (Forfivo XL)
Desvenlafaxine extended-release tablet (Khedezla ER)
Desvenlafaxine fumarate extended-release tablet
Desvenlafaxine succinate extended-release tablet (Pristiq ER)
Duloxetine HCl (Cymbalta)
Fluoxetine HCl 10mg, 15mg, 20mg Tablet; 40mg capsule; and 90mg
weekly capsule (Prozac)
Fluvoxamine maleate extended-release (Luvox CR)
Milnacipran HCl (Savella)
Mirtazapine 7.5 mg Tablet, and orally disintegrating tablet (Remeron
SolTab)
Nefazodone HCl (Serzone)
Paroxetine HCl controlled-release tablet, and 10mg/5ml suspension
(Paxil)
Paroxetine mesylate (Pexeva)
Vilazodone HCl (Viibryd)
Vortioxetine HBr (Brintellix)
Nonpreferred agents

Levomilnacipran HCl extended-release tablet (Fetzima ER)
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria

Paroxetine mesylate (Brisdelle)
Exempt SGAD combination agents with criteria
Fluoxetine HCL/Olanzapine (Symbyax)
Approval criteria for preferred or exempt agents
Drug daily dose ≤ maximum daily dose (Table 1)
Approval criteria for preferred or exempt agents resulting from a
therapeutic duplication


If applicable for a change in therapy or concomitant therapy of two agents and
only one or neither are SSRIs and/or SSNRIs (including combinations) (Table
1.2):
 Drug in history reflects a minimal therapeutic dose (Table 1) for at least
four weeks
OR
If applicable for a change in therapy for two SSRIs and/or SSNRIs (including
combinations) (Table 1.2)
 Drug in history reflects a minimal therapeutic dose (Table 1) for at least
four weeks, AND
 No prior therapeutic duplication for two different SSRIs and/or SSNRIs
(including combinations) (Table 1.2) within the past 365 days.
Approval criteria for all nonpreferred agents except milnacipran
> 90 days of therapy in the previous 120 days for the same drug, strength, and
daily dose with the denial exception of a therapeutic duplication between an
SSRI and/or SNRI between incoming claim and history
Denial criteria for all agents



Preferred agents or exempt agents
 Therapeutic duplication of three agents
 Therapeutic duplication of two SSRIs and/or SSNRIs (including
combinations) (Table 1.2) more than once per 365 days
Nonpreferred drugs for patients who do not meet criteria of >90 days of
therapy in the previous 120 days for the same drug, strength, and daily dose
See Fibromyalgia agents for additional criteria on select second generation
antidepressants
Link to PDL Memorandum: Second Generation Antidepressants
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Table 1 – Minimum and maximum dose for second-generation
antidepressants
Drug
Bupropion
Citalopram
Desvenlafaxine
Duloxetine
Escitalopram
Fluoxetine
Fluoxetine/olanzapine*
Fluvoxamine
Mirtazapine
Nefazodone
Paroxetine
Sertraline
Venlafaxine
Minimal daily therapeutic dose
200mg
20mg
50mg
40mg
10mg
20mg
25mg
100mg
30mg
300mg
30mg
100mg
150mg
Maximum daily dose
450mg
40mg
100mg
60mg
30mg
80mg
75mg
300mg
60mg
600mg
60mg (CR 62.5mg)
200mg
375mg
* Minimum therapeutic dose and maximum dose based on SSRI component of the
combination agent.
Table 1.2 – Selective Serotonin (norepinephrine) Reuptake
Inhibitors (combinations)
SSRI, SSNRI or SSRI Combinations
Citalopram
Desvenlafaxine
Duloxetine
Escitalopram
Fluoxetine
Fluoxetine/olanzapine
Fluvoxamine
Paroxetine
Sertraline
Venlafaxine
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Antidiabetic Agents
(Implemented 01/01/2009)
Prescribers may request an override for nonpreferred drugs by calling the
UAMS College of Pharmacy Evidence-Based Prescription Drug Program
Help Desk at 1-866-250-2518 (toll-free) or 501-526-4200 (local).
Preferred agents







Glimepiride (Amaryl)
Glipizide (Glucotrol)
Glipizide extended-release (Glucotrol XL)
Glipizide/Metformin HCl (Metaglip)
Glyburide (Diabeta, Glynase Prestab)
Glyburide/Metformin HCl (Glucovance)
Nateglinide (Starlix)
Non-Preferred agents

























Albiglutide (Tanzeum)
Alogliptin benzoate (Nesina)
Alogliptin benzoate/Metformin HCl (Kazano)
Alogliptin benzoate/Pioglitazone (Oseni)
Canagliflozin (Invokana)
Canagliflozin/Metformin (Invokamet)
Dapagliflozin (Farxiga)
Dapagliflozin/Metformin HCl (Xigduo XR)
Dulaglutide (Trulicity)
Empagliflozin (Jardiance)
Exenatide (Byetta)
Exenatide microspheres (Bydureon)
Linagliptin (Tradjenta)
Linagliptin/Metformin HCl (Jentadueto)
Liraglutide (Victoza)
Pioglitazone HCl (Actos)
Pioglitazone HCl/Glimepiride (Duetact)
Pioglitazone HCl/ Metformin HCl (Actoplus Met)
Pramlintide Acetate (Symlin, SymlinPen)
Repaglinide (Prandin)
Repaglinide/Metformin HCl (Prandimet)
Rosiglitazone (Avandia)
Rosiglitazone/Glimepiride (Avandaryl)
Rosiglitazone/Metformin HCl (Avandamet)
Saxagliptin HCl (Onglyza)
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria





Saxagliptin HCl/Metformin HCl (Kombiglyze XR)
Sitagliptin Phosphate (Januvia)
Sitagliptin phosphate/Metformin HCl (Janumet)
Sitagliptin phosphate/Metformin HCl extended-release (Janumet XR)
Sitagliptin phosphate/Simvastatin (Juvisync)
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Anti-inflammatory Ophthalmic Drops
(Implemented 01/12/2010)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
History of at least two claims for two different products that do not require prior
authorization within the previous 28 days
ANTI-INFLAMMATORY OPHTHALMIC DROPS
GENERIC NAME
COMMON TRADE NAME*
PA STATUS
Dexamethasone Sodium Phosphate 0.1% eye drops
Decadron® 0.1% eye drops
No PA
Diclofenac 0.1% eye drops
Voltaren® 0.1% eye drops
No PA
Fluorometholone 0.1% eye drops
FML Liquifilm® 0.1% eye drops
No PA
Fluorometholone 0.25% eye drops
FML Forte® 0.25% eye drops
No PA
Flurbiprofen 0.03% eye drops
Ocufen® 0.03% eye drops
No PA
Ketorolac 0.5% eye drops
Acular® 0.5% eye drops
No PA
Ketorolac 0.4% eye drops
Acular LS® 0.4% eye drops
No PA
Prednisolone acetate 1% eye drops
Pred Forte® 1% eye drops
No PA
Prednisolone acetate 0.12% eye drops
Pred Mild® 0.12% eye drops
No PA
Prednisolone sodium 1% eye drops
AK-Pred® 1% eye drops
No PA
GENERIC NAME
COMMON TRADE NAME*
PA STATUS
Bromfenac 0.07% eye drops
Prolensa® 0.07% eye drops
PA
Bromfenac 0.09% eye drops
Bromday® 0.09% eye drops
PA
Dexamethasone 0.1% suspension eye drops
Maxidex® 0.1% suspension eye drops
PA
Difluprednate 0.05% eye drops
Durezol® 0.05% eye drops
PA
Fluorometholone 0.1% eye drops
Flarex® 0.1% eye drops
PA
Ketorolac 0.45% eye drops
Acuvail® 0.45% eye drops
PA
Loteprednol 0.2% eye drops
Alrex® 0.2% eye drops
PA
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Loteprednol 0.5% eye drops
Lotemax® 0.5% eye drops
PA
Loteprednol 0.5% eye gel drops
Lotemax® 0.5% eye gel drops
PA
Nepafenac 0.1% eye drops
Nevanac® 0.1% eye drops
PA
Nepafenac 0.3% eye drops
Ilevro® 0.3% eye drops
PA
Rimexolone 1% eye drops
Vexol® 1% eye drops
PA
*TRADE NAMES ARE FOR REFERENCE ONLY
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Nonsteroidal Anti-inflammatory Agents
(Implemented 06/18/2007)
Prescribers may request an override for nonpreferred drugs by calling the
UAMS College of Pharmacy Evidence-Based Prescription Drug Program
Help Desk at 1-866-250-2518 (toll-free) or 501-526-4200 (local).
Preferred agents









Diclofenac sodium ER 100mg tablet (Voltaren XR)
Ibuprofen 100mg/5ml suspension; 400mg, 600mg, 800mg tablet (Motrin)
Indomethacin 25mg, 50mg capsule (Indocin)
Ketoprofen 50mg, 75mg capsule (Orudis)
Meloxicam 7.5mg, 15mg tablet (Mobic)
Naproxen 250mg, 375mg, 500mg tablet (Naprosyn)
Naproxen 375mg, 500mg enteric-coated tablet (EC-Naprosyn)
Naproxen sodium 275mg and 550mg tablet (Anaprox)
Salsalate 750mg (Salflex-750)
Preferred agent with criteria

Ketorolac tablet (Toradol)
Nonpreferred agents




















Celecoxib (Celebrex)
Diclofenac epolamine (Flector)
Diclofenac potassium (Cambia, Cataflam, Zipsor)
Diclofenac sodium 25mg, 50mg, and 75 mg tablet (Voltaren)
Diclofenac sodium topical (Pennsaid, Voltaren Gel)
Diclofenac sodium/Misoprostol (Arthrotec)
Diclofenac submicronized (Zorvolex)
Diflunisal (Dolobid)
Etodolac (Lodine)
Fenoprofen (Nalfon)
Flurbiprofen (Ansaid)
Ibuprofen 40mg/ml suspension; 50mg,100mg tablet (Motrin)
Ibuprofen/caffeine/B1/B2/B6/B12 (IC400, IC800 Kit)
Ibuprofen/famotidine (Duexis)
Indomethacin 75mg SA Capsule; 50mg suppository; 25mg/5ml
suspension (Indocin)
Ketoprofen 200mg extended-release capsule (Oruvail)
Ketorolac nasal spray (Sprix)
Meclofenemate sodium (Meclomen)
Mefenamic acid (Ponstel)
Meloxicam suspension (Mobic)
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria









Nabumetone (Relafen)
Naproxen/Esomeprazole magnesium (Vimovo)
Naproxen Suspension (Naprosyn)
Naproxen sodium 375mg and 500mg extended-release tablet (Naprelan)
Oxaprozin (Daypro)
Piroxicam (Feldene)
Salsalate 500mg (Salflex-500)
Sulindac (Clinoril)
Tolmetin sodium (Tolectin)
Nonpreferred agents with criteria


Diclofenac Sodium 3% Gel (Solaraze)
Naproxen 125mg/ml suspension (Naprosyn suspension)
Approval criteria for nonpreferred agents with criteria
 Diclofenac Sodium 3% Gel (Soloraze)
 Diagnosis of Actinic Keratosis in the past two months
 Naproxen 125mg/ml suspension (Naprosyn suspension)
 < 6 years of age, OR
 NPO (Appendix A)
Denial criteria for preferred agent with criteria

Ketorolac
o History of ketorolac use in the last 60 days, OR
o NSAID claim in the past 30 days, OR
o Dose greater than four per day, OR
o Day supply greater than five, OR
o Quantity greater than 20, OR
o Greater than 20 units per 60 days
Link to PDL Memorandum: NSAIDS
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Antihistamine Eye Drops, Mast Cell Stabilizers, and
combination Mast Cell Stabilizer-Antihistamine Eye
Drops
(Implemented 01/12/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
EYE DROPS FOR ALLERGIC CONJUNCTIVITIS
GENERIC NAME
COMMON TRADE NAME*
PA STATUS
Azelastine HCl 0.05% eye drops
Optivar® 0.05% eye drops
No PA
Cromolyn sodium 4% eye drops
Cromolyn® 4% eye drops
No PA
Ketotifen fumarate 0.025% eye drops
Alaway® 0.025% eye drops
No PA
Ketotifen fumarate 0.025% eye drops
Zaditor® 0.025% eye drops
No PA
GENERIC NAME
COMMON TRADE NAME*
PA STATUS
Alcaftadine 0.25% eye drops
Lastacaft® 0.25% eye drops
Manual PA
Bepotastine besilate 1.5% eye drops
Bepreve® 1.5% eye drops
Manual PA
Emedastine difumarate 0.05% eye drops
Emadine® 0.05% eye drops
Manual PA
Epinastine HCl 0.05% eye drops
Elestat® 0.05% eye drops
Manual PA
Lodoxamide tromethamine 0.1% eye drops
Alomide® 0.1% eye drops
Manual PA
Nedocromil sodium 2% eye drops
Alocril® 2% eye drops
Manual PA
Olopatadine HCl 0.1% eye drops
Patanol® 0.1% eye drops
Manual PA
Olopatadine HCl 0.2% eye drops
Pataday® 0.2% eye drops
Manual PA
Pemirolast potassium 0.1% eye drops
Alamast® 0.1% eye drops
Manual PA
*TRADE NAMES ARE FOR REFERENCE ONLY
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Second-generation Antihistamines
(Implemented 11//2007)
Prescribers may request an override for nonpreferred drugs by calling the
UAMS College of Pharmacy Evidence-Based Prescription Drug Program
Help Desk at 1-866-250-2518 (toll-free) or 501-526-4200 (local).
Preferred agents



Cetirizine HCl 1 mg/ml solution, 10 mg swallow tablet (Zyrtec)
Loratadine (Claritin)
Olopatadine HCl 6% nasal spray (Patanase)
Nonpreferred agents




Acrivastine w/Pseudoephedrine (Semprex-D)
Azelastine HCL nasal spray (Astelin, Astepro)
Azelastine/fluticasone nasal spray (Dymista)
Desloratidine liquid (Clarinex)
Nonpreferred agents with criteria




Cetirizine
 Cetirizine 5 mg, 10 mg chewable tablet (Zyrtec)
 Cetirizine w/Pseudoephedrine (Zyrtec-D)
Desloratadine
 Desloratadine tablet (Clarinex)
 Desloratadine w/Pseudoephedrine tablet (Clarinex-D)
Fexofenadine
 Fexofenadine (Allegra)
 Fexofenadine w/Pseudoephedrine (Allegra-D)
Levocetirizine (Xyzal)
Approval criteria for nonpreferred agents with criteria

All nonpreferred drugs with criteria
 > Four claims for the drug, strength and dosage form of any
nonpreferred drug in the last six months
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Topical Antifungals
(Implemented 09/21/2009)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
History of at least two claims for two different topical antifungal products
containing different drug entities that do not require prior authorization within the
previous 45 days.
TOPICAL ANTIFUNGALS
GENERIC NAME
COMMON TRADE NAME*
PA STATUS
Ciclopirox 0.77% cream
Loprox® 0.77% cream
No PA
Ciclopirox 0.77% topical suspension
Loprox® 0.77% topical suspension
No PA
Clotrimazole 1% cream (OTC or Rx)
Lotrimin AF® 1% cream
No PA
Clotrimazole 1% solution
Lotrimin® 1% solution
No PA
Econazole nitrate 1% cream
Spectazole® 1% cream
No PA
Ketoconazole 2% cream
Nizoral® 2% cream
No PA
Ketoconazole 2% shampoo
Nizoral® 2% shampoo
No PA
GENERIC NAME
COMMON TRADE NAME*
PA STATUS
Butenafine HCl 1% cream
Mentax® 1% cream
PA
Ciclopirox 0.77% gel
Loprox® 0.77% gel
PA
Ciclopirox 1% shampoo
Loprox® 1% shampoo
PA
Ketoconazole 2% foam
Extina® 2% foam
PA
Ketoconazole 2% gel
Xolegel 2% gel
PA
Luliconazole 1% cream
Luzu® 1% cream
PA
Naftifine HCl 1% cream
Naftin® 1% cream
PA
Naftifine HCl 1% cream
Naftin® 1% pump cream
PA
Naftifine HCl 1% gel
Naftin® 1% gel
PA
Naftifine HCl 2% cream
Naftin® 2% cream
PA
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Naftifine HCl 2% gel
Naftin® 2% gel
PA
Oxiconazole nitrate 1% cream
Oxistat® 1% cream
PA
Oxiconazole nitrate 1% lotion
Oxistat® 1% lotion
PA
Sertaconazole nitrate 2% cream
Ertaczo® 2% cream
PA
Sulconazole nitrate 1% cream
Exelderm® 1% cream
PA
Sulconazole nitrate 1% solution
Exelderm® 1% solution
PA
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Antipsychotics, Injectable Long-acting
(Implemented 01/12/2010)
Prescribers may request an override by calling the UAMS College of
Pharmacy Evidence-Based Prescription Drug Program Help Desk at 1-866250-2518 (toll-free) or 501-526-4200 (local).
Approval criteria
All injectable long acting antipsychotics (Abilify MaintenaTM, fluphenazine
decanoate, haloperidol decanoate, Risperdal® Consta®, Invega® Sustenna®,
Zyprexa® RelprevvTM):


Absence of denial criteria
Age < 18 years requires Manual Review
Additional criteria:
Abilify MaintenaTM
 Three paid claims for oral AbilifyTM in the past 14-75 days at a dose of >/=
10 mg/day, OR
 One paid claim for Abilify MaintenaTM in the past 45 days
Invega® Sustenna®
 Two paid claims for oral Invega® in the past 27-75 days, OR
 Two paid claims for oral Risperdal® in the past 27-75 days, OR
 One paid claim for Invega® Sustenna® in the past 45 days
Risperdal® Consta®
 Two paid claims for oral Risperdal® in the past 27-75 days, OR
 Two paid claims for oral Invega® in the past 27-75 days, OR
 One paid claim for Risperdal® Consta® in the past 45 days
Zyprexa® RelprevvTM Injection
 Two paid claims for oral Zyprexa® in the past 27-75 days, OR
 One paid claim for Zyprexa® RelprevvTM in the past 45 days
Denial criteria
All injectable long acting antipsychotics
 Therapeutic duplication with another long acting antipsychotic in the past
23 days
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Antipsychotics, Oral
(Implemented 07/11/2009)
Prescribers may request an override by calling the UAMS College of
Pharmacy Evidence-Based Prescription Drug Program Help Desk at 1-866250-2518 (toll-free) or 501-526-4200 (local).
Approval criteria
Patients ≥ 18 years of age
 Oral liquids and orally disintegrating tablets (ODTs): Patient must have an
NPO code (Appendix A) in the past year
 Oral capsules/tablets are approved
 Seroquel XR requires >/= 90 days of Seroquel XR therapy in the past 120
days. Immediate-release quetiapine (Seroquel) is covered via existing
criteria.
Patients < 18 years of age
 At least one paid claim for an oral antipsychotic in the past 45 days, and
monitoring for both glucose and lipid screening in the past 9 months
(Table 2.3)
 Typical and Atypical antipsychotics:
o All new start patients or patients changed to a different chemical
entity will require a signed informed consent and a copy of a baseline
metabolic lab test data. (Effective 11/8/2011)
Medication Informed Consent Document
o One therapeutic duplication for a change in therapy between two
antipsychotics (oral or injectable) with > 25% remaining on the last fill
on different dates of service allowed per 93 days.
o PA required through manual review for recipients < 6 years of age.
 Oral liquids and orally disintegrating tablets (ODTs): Patient must have an
NPO code (Appendix A) in the past year OR be < 7 years of age AND
meet criteria for atypical antipsychotics
 Seroquel XR requires >/= 90 days of Seroquel XR therapy in the past
120 days. Immediate-release quetiapine (Seroquel) is covered via
existing criteria.
Additional dose criteria
Atypical antipsychotics
 Requested dose must be an approved dose for age range (Table 2)
 Requested maximum daily dose must be approved for age range (Table
2.2).
Denial criteria
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Antipsychotics
 Claims with a therapeutic duplication on the same date of service
 Requests for Loxapine, Thioridazine, Thiothixene, Fanapt®, Latuda®, or
Saphris® for patients <18 years of age
 Requests for combination antipsychotic products for patients <18 years
of age
 Failure to meet approval criteria
Table 2 – Approved doses per age range
Drug
Abilify®
Abilify®
Abilify®
Abilify®
Abilify®
Abilify®
Abilify Dismelt®
Abilify Dismelt®
Abilify Solution®
Chlorpromazine
Chlorpromazine
Chlorpromazine
Chlorpromazine
Chlorpromazine
Fanapt®
Fanapt®
Fanapt®
Fanapt®
Fanapt®
Fanapt®
Fanapt®
Fluphenazine
Fluphenazine
Fluphenazine
Fluphenazine
Fluphenazine Elixir
Fluphenazine Soln
Geodon®
Geodon®
Geodon®
Geodon®
Strength
2 mg
5 mg
10 mg
15 mg
20 mg
30 mg
10 mg
15 mg
1 mg/ml
10 mg
25 mg
50 mg
100 mg
200 mg
1 mg
2 mg
4 mg
6 mg
8 mg
10 mg
12 mg
1 mg
2.5 mg
5 mg
10 mg
2.5mg/5ml
5 mg/ml
20 mg
40 mg
60 mg
80 mg
FDA
dosing
QD
QD
QD
QD
QD
QD
QD
QD
QD
BID-QID
BID-QID
BID-QID
BID-QID
BID-QID
BID
BID
BID
BID
BID
BID
BID
BID-QID
BID-QID
BID-QID
BID-QID
BID-QID
BID-QID
BID
BID
BID
BID
<6* y/o
2 tabs
1 tab
6-9 y/o
2 tabs
1 tab
1 tab
1 tab
10-12y/o
2 tabs
1 tab
1 tab
1 tab
1 tab
1 tab
1 tab
15 mls
4 tabs
4 tabs
4 tabs
2 tabs
1 tab
2 tabs
2 tabs
1 tab
2 tabs
1 tab
20 mls
4 tabs
4 tabs
4 tabs
4 tabs
2 tabs
2 tabs
2 tabs
2 tabs
1 tab
1 tab
2 tabs
4 tabs
2 tabs
1 tab
4 mls
0.4 ml
2 caps
10 mls
1 ml
2 caps
1 cap
1 cap
4 tabs
4 tabs
2 tabs
1 tab
20 mls
2 mls
2 caps
2 caps
5 mls
4 tabs
4 tabs
2 tabs
1 tab
2 tabs
1 tab
1317y/o
2 tabs
1 tab
1 tab
1 tab
1 tab
1 tab
2 tabs
2 tabs
30 mls
4 tabs
4 tabs
4 tabs
4 tabs
3 tabs
2 tabs
2 tabs
2 tabs
2 tabs
2 tabs
1 tab
1 tab
4 tabs
4 tabs
4 tabs
2 tabs
40 mls
4 mls
2 caps
2 caps
2 caps
2 caps
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Drug
Haloperidol
Haloperidol
Haloperidol
Haloperidol
Haloperidol
Haloperidol
Haloperidol Soln
Invega®
Invega®
Invega®
Invega®
Latuda®
Latuda®
Latuda®
Latuda®
Latuda®
Loxapine
Loxapine
Loxapine
Loxapine
Orap®
Orap®
Perphenazine
Perphenazine
Perphenazine
Perphenazine
Risperdal®
Risperdal®
Risperdal®
Risperdal®
Risperdal®
Risperdal®
Risperdal® M Tab
Risperdal® M Tab
Risperdal® M Tab
Risperdal® M Tab
Risperdal® M Tab
Risperdal® M Tab
Risperdal® Soln
Saphris® SL
Saphris® SL
Seroquel®
Seroquel®
Strength
0.5 mg
1 mg
2 mg
5 mg
10 mg
20 mg
2 mg/ml
1.5 mg
3 mg
6 mg
9 mg
20 mg
40 mg
60 mg
80 mg
120 mg
5 mg
10 mg
25 mg
50 mg
1 mg
2 mg
2 mg
4 mg
8 mg
16 mg
0.25 mg
0.5 mg
1 mg
2 mg
3 mg
4 mg
0.25 mg
0.5 mg
1 mg
2 mg
3 mg
4 mg
1 mg/ml
5 mg
10 mg
25 mg
50 mg
FDA
dosing
BID-TID
BID-TID
BID-TID
BID-TID
BID-TID
BID-TID
BID-TID
QD
QD
QD
QD
QD
QD
QD
QD
QD
BID
BID
BID
BID
QD-BID
QD-BID
BID-QID
BID-QID
BID-QID
BID-QID
BID
BID
BID
BID
BID
BID
BID
BID
BID
BID
BID
BID
BID
BID
BID
TID
TID
<6* y/o
3 tabs
2 tabs
1 tab
6-9 y/o
3 tabs
3 tabs
2 tabs
1 tab
10-12y/o
3 tabs
3 tabs
3 tabs
2 tabs
1 tab
1 ml
1 tab
1 tab
2.5 ml
1 tab
1 tab
5 ml
1 tab
1 tab
1 tab
1 tab
1 tab
1 tab
1 tab
1 tab
2 caps
1 cap
2 caps
2 caps
2 caps
2 caps
1 tab
2 tabs
1 tab
1 tab
1 tab
3 tabs
1 tab
1 tab
2 tabs
4 tabs
2 tabs
1 tab
2 tabs
2 tabs
2 tabs
1 tab
2 tabs
2 tabs
2 tabs
2 tabs
2 tabs
2 tabs
2 tabs
1 tab
1 tab
2 tabs
2 tabs
2 tabs
2 tabs
2 mls
1 tab
1 tab
4 mls
1 tab
3 tabs
3 tabs
3 tabs
3 tabs
2 tabs
2 tabs
2 tabs
2 tabs
2 tabs
1 tab
2 tabs
2 tabs
2 tabs
2 tabs
2 tabs
1 tab
6 mls
2 tabs
1 tab
3 tabs
3 tabs
1317y/o
3 tabs
3 tabs
3 tabs
3 tabs
2 tabs
1 tab
10 ml
1 tab
1 tab
1 tab
1 tab
1 tab
1 tab
1 tab
1 tab
2 caps
2 caps
2 caps
1 cap
1 tab
5 tabs
4 tabs
4 tabs
2 tabs
1 tab
2 tabs
2 tabs
2 tabs
2 tabs
2 tabs
2 tabs
2 tabs
2 tabs
2 tabs
2 tabs
2 tabs
2 tabs
8 mls
2 tabs
2 tabs
3 tabs
3 tabs
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Drug
Seroquel®
Seroquel®
Seroquel®
Seroquel®
Seroquel® XR
Seroquel® XR
Seroquel® XR
Seroquel® XR
Seroquel® XR
Thioridazine
Thioridazine
Thioridazine
Thioridazine
Thiothixene
Thiothixene
Thiothixene
Thiothixene
Trifluoperazine
Trifluoperazine
Trifluoperazine
Trifluoperazine
Zyprexa®
Zyprexa®
Zyprexa®
Zyprexa®
Zyprexa®
Zyprexa®
Zyprexa® Zydis®
Zyprexa® Zydis®
Zyprexa® Zydis®
Zyprexa® Zydis®
Strength
100 mg
200 mg
300 mg
400 mg
50 mg
150 mg
200 mg
300 mg
400 mg
10 mg
25 mg
50 mg
100 mg
1 mg
2 mg
5 mg
10 mg
1 mg
2 mg
5 mg
10 mg
2.5mg
5mg
7.5mg
10mg
15mg
20mg
5mg
10mg
15mg
20mg
FDA
dosing
TID
TID
TID
TID
QD
QD
QD
QD
QD
BID-TID
BID-TID
BID-TID
BID-TID
TID
TID
TID
TID
QD-BID
QD-BID
QD-BID
QD-BID
QD
QD
QD
QD
QD
QD
QD
QD
QD
QD
<6* y/o
1 tab
6-9 y/o
3 tabs
1 tab
1 tab
2 tabs
1 tab
2 tabs
1 tab
1 tab
1 tab
3 tabs
2 tabs
1 tab
3 tabs
3 tabs
2 tabs
1 tab
3 caps
3 caps
1 cap
3 caps
3 caps
1 cap
10-12y/o
3 tabs
3 tabs
2 tabs
1 tab
2 tabs
1 tab
1 tab
2 tabs
1 tab
3 tabs
3 tabs
3 tabs
1 tab
3 caps
3 caps
1 cap
1 tab
2 tabs
1 tab
2 tabs
2 tabs
1 tab
1 tab
1 tab
1 tab
1 tab
1 tab
1 tab
1 tab
1 tab
1 tab
1 tab
1 tab
1 tab
1 tab
1 tab
1 tab
1 tab
1 tab
1317y/o
3 tabs
3 tabs
2 tabs
2 tabs
2 tabs
1 tab
1 tab
2 tabs
2 tabs
3 tabs
3 tabs
3 tabs
2 tabs
3 caps
3 caps
3 caps
1 cap
2 tabs
2 tabs
2 tabs
1 tab
1 tab
1 tab
1 tab
1 tab
1 tab
1 tab
1 tab
1 tab
1 tab
1 tab
*Prior authorization required through manual review for recipients < 6 years of age.
Table 2.2 – Max daily doses for age categories < 18 years of age.
Drug
Abilify®
Geodon®
Invega®
Risperdal®
<6* y/o
5 mg daily
40 mg daily
3 mg daily
2 mg daily
6*-9 y/o
15 mg daily
60 mg daily
3 mg daily
4 mg daily
10-12 y/o
20 mg daily
80 mg daily
6 mg daily
6 mg daily
13-17 y/o
30 mg daily
160 mg daily
9 mg daily
8 mg daily
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Drug
Seroquel®
Zyprexa®
<6* y/o
150 mg daily
5 mg daily
6*-9 y/o
300 mg daily
10 mg daily
10-12 y/o
600 mg daily
15 mg daily
13-17 y/o
800 mg daily
20 mg daily
*Prior authorization required through manual review for recipients < 6 years of age.
Table 2.3 – CPT codes for glucose and lipid monitoring.
Glucose codes: Criteria require one of the following CPT codes that contain
glucose monitoring in the previous 9 months from claim date of in-process claim:
 83036 (HbA1c), OR
 80050 (General Health Panel), OR
 80069 (Renal Function Panel), OR
 80047 (Basic Metabolic Panel), OR
 80048 (Basic Metabolic Panel), OR
 80053 (Comprehensive metabolic panel ), OR
 82962 (Glucose, blood by glucose monitoring device(s) cleared by
the FDA specifically for home use) OR
 82948 (Glucose; blood, reagent strip ) OR
 82947 (Glucose; quantitative, blood),
AND, criteria require one of the following lipid panel tests or all of the
individual lipid test monitoring codes in previous 9 months from claim date
of the in-process claim:
Lipid codes:
 80061 (Lipid panel ), OR
 83701 (High resolution fractionation and quantitation of lipoproteins
panel), OR
 82465 (Cholesterol, serum or whole blood, total ), AND 83718 (HDL
cholesterol ), AND 84478 (Triglycerides ), AND 83721 (LDL Cholesterol)
Link to Memorandum (Initial Antipsychotic criteria)
Link to Memorandum (Requirements of informed consent and metabolic
monitoring)
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Apixaban Tablet (Eliquis)
(Implemented 07/09/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria




Diagnosis for Atrial Fibrillation in Medicaid history within past 2 years;
No Therapeutic duplication allowed between different strengths of
Eliquis®;
One (1) therapeutic duplication with overlapping days’ supply will be
allowed once per 186 days for inferred change in therapy between an
Eliquis® claim and any of the following: a Xarelto® claim, a warfarin
claim, OR a Pradaxa® claim, AND
The Eliquis® claim and the warfarin claim, the Xarelto® claim, or the
Pradaxa® claim cannot have the same date of service.
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Armodafinil (Nuvigil)
(Implemented 05/27/2009)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria


Age > 16 years of age, AND
History of at least one of the following in the last two years:
o Narcolepsy, OR
o Multiple sclerosis, OR
o Shift work sleep disorder, OR
o Obstructive sleep apnea/hypopnea, AND
 CPAP, OR
 BPAP, OR
 Nasal interface positive airway pressure device
Denial criteria


Age < 16 years of age, OR
History of at least one of the following in the last 30 days:
o Atomoxetine (Strattera), OR
o CII Stimulants, OR
o Other modafinil (Provigil) strengths, OR
o Other armodafinil (Nuvigil) strengths, OR
o Pemoline (Cylert)
Additional criteria
Quantity limits apply
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Aromatase Inhibitors (Arimidex and Femara)
(Implemented 09/24/2008)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require prior authorization


Anastrozole oral tablet [Arimidex]
Letrozole oral tablet [Femara]
Approval criteria
Medical history for female metastatic breast cancer in the past 3 years
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Attention Deficit Disorder and Attention Deficit
Hyperactivity Disorder (ADD/ADHD) Agents for
Children (Less than 18 Years of Age)
(Implemented 07/21/2009)
Prescribers may request an override for nonpreferred drugs by calling the
UAMS College of Pharmacy Evidence-Based Prescription Drug Program
Help Desk at 1-866-250-2518 (toll-free) or 501-526-4200 (local).
Preferred agents with criteria








Adderall XR (Brand only)
Amphetamine salts immediate-release tablet (Adderall)
Atomoxetine HCl (Strattera)
Dextroamephetamine sulfate 5mg, 10mg tablet (Dextrostat)
Focalin (Brand only)
Focalin XR (Brand only)
Lisdexamfetamine dimesylate (Vyvanse)
Methylphenidate HCl swallow tablet (Ritalin)
Nonpreferred agents

















Amphetamine salts extended-release capsule (generic Adderall XR)
Clonidine extended-release suspension (Nexiclon XR)
Clonidine extended-release tablet (Kapvay ER, Nexiclon XR)
Dexmethylphenidate HCl extended-release capsule (generic Focalin XR)
Dexmethylphenidate HCl tablet (generic Focalin)
Dextroamephetamine sulfate extended-release capsule (Dexedrine
Spansule)
Dextroamphetamine sulfate solution (Liquadd, Procentra)
Dextroamphetamine sulfate 2.5mg, 7.5mg tablet (Zenzedi)
Guanfacine HCl extended-release tablet (Intuniv ER)
Methamphetamine HCl (Desoxyn)
Methylphenidate HCl chewable tablet (Methylin)
Methylphenidate HCl extended-release capsule (Metadate CD, Ritalin LA)
Methylphenidate extended-release patch (Daytrana)
Methylphenidate HCl extended-release suspension (Quillivant XR)
Methylphenidate HCl extended-release tablet (Concerta)
Methylphenidate HCl extended-release tablet (Metadate ER, Ritalin SR)
Methylphenidate HCl solution (Methylin)
Approval criteria for preferred agents with criteria for children:
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Less than18 years of age
All preferred extended-release CII stimulants:
 ≤ One therapeutic duplication between long-acting CII stimulants with 75%
of the last fill per 93 days AND
 If a incoming long-acting CII stimulant claim overlaps with a short-acting CII
stimulant that was filled at a dose of >/= to 2 units per day, the long-acting
product will require prior authorization
All preferred immediate-release CII stimulants:
 ≤ One therapeutic duplication between short-acting CII stimulants with 75%
of the last fill per 93 days AND
 If an incoming short-acting CII stimulant claim overlaps with a long-acting
CII stimulant, the short-acting product will only be approved for a dose of
one unit per day
Additional criteria
Age and Quantity limits apply
Link to orginal Memorandum
Link to current Memorandum with new quantity restrictions
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Attention Deficit Disorder and Attention Deficit
Hyperactivity Disorder (ADD/ADHD) Agents for Adults
(18 Years of Age or greater)
(Implemented 01/18/2011)
Preferred agents with criteria








Adderall XR (Brand only)
Amphetamine salts immediate-release tablet (Adderall)
Atomoxetine HCl (Strattera)
Dextroamephetamine sulfate 5mg, 10mg tablet (Dextrostat)
Focalin (Brand only)
Focalin XR (Brand only)
Lisdexamfetamine dimesylate (Vyvanse)
Methylphenidate HCl swallow tablet (Ritalin)
Nonpreferred agents

















Amphetamine salts extended-release capsule (generic Adderall XR)
Clonidine extended-release suspension (Nexiclon XR)
Clonidine extended-release tablet (Kapvay ER, Nexiclon XR)
Dexmethylphenidate HCl extended-release capsule (generic Focalin XR)
Dexmethylphenidate HCl tablet (generic Focalin)
Dextroamephetamine sulfate extended-release capsule (Dexedrine
Spansule)
Dextroamphetamine sulfate solution (Liquadd, Procentra)
Dextroamphetamine sulfate 2.5mg, 7.5mg tablet (Zenzedi)
Guanfacine HCl extended-release tablet (Intuniv ER)
Methamphetamine HCl (Desoxyn)
Methylphenidate HCl chewable tablet (Methylin)
Methylphenidate HCl extended-release capsule (Metadate CD, Ritalin LA)
Methylphenidate extended-release patch (Daytrana)
Methylphenidate HCl extended-release suspension (Quillivant XR)
Methylphenidate HCl extended-release tablet (Concerta)
Methylphenidate HCl extended-release tablet (Metadate ER, Ritalin SR)
Methylphenidate HCl solution (Methylin)
Approval criteria for preferred agents with criteria for adults:
18 years of age or greater


Diagnosis of Narcolepsy in Medicaid History in the previous 2 years and
No therapeutic duplication with a different ADD/ADHD with different GCN in
history with > 25% remaining days supply
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria


No therapeutic duplication with a Provigil/Nuvigil in history with > 25%
remaining days supply
No therapeutic duplication with Atomoxetine in history with > 25% remaining
days supply
Atomoxetine for adults (18 years of age or greater)

Required for all new starts with no diagnosis of Narcolepsy in Medicaid
history.
Denial criteria for adults (18 years of age or greater)

No Diagnosis of Narcolepsy in Medicaid History in the previous 2 years will
require a manual review
Additional criteria
Quantity limits apply
Link to Memorandum: CII Stimulant for Adults
Link to current Memorandum with new quantity restrictions
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Auranolfin (Ridaura) Capsule
(Implemented 09/18/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Ridaura Capsule
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Axitinib Tablet (Inlyta)
(Implemented 07/09/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Inlyta tablet
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Azithromycin (Azithromycin Powder Packets and
ZMAX)
(Implemented 04/12/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Azithromycin 1 gm powder packets

ZMAX 2gm/60ml suspension
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Aztreonam Inhalation Solution (Cayston)
(Implemented 09/28/2010)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Cayston Inhalation Solution
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Balsalazide Disodium Tablet (Giazo)
(Implemented 07/09/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Giazo
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Becaplermin (Regranex)
(Implemented 01/12/2005)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria


Submitted ICD-9 diagnosis of diabetes mellitus in past 365 days, AND
Submitted ICD-9 diagnosis of skin ulcer in past 180 days
Denial criteria


Submitted ICD-9 diagnosis of osteomyelitis in past 90 days, OR
> one claim in past 30 days
Additional criteria
Quantity limits apply
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Bedaquiline Fumarate Tablet (Sirturo)
(Implemented 12/10/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Sirturo
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Belimumab (Benlysta)
(Implemented 06/21/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Benlysta
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Benign Prostatic Hypertrophy (BPH) Drugs
(Implemented 01/12/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
BENIGN PROSTATIC HYPERTROPHY (BPH) DRUGS
GENERIC NAME
COMMON TRADE NAME*
PA STATUS
Alfuzosin HCl ER 10 mg tablet
Uroxatral® 10 mg tablet
No PA
Finasteride 5 mg tablet
Proscar 5® mg tablet
See Finasteride
Tamsulosin HCl 0.4 mg capsule
Flomax® 0.4 mg capsule
No PA
GENERIC NAME
COMMON TRADE NAME*
PA STATUS
Dutasteride 0.5 mg softgel
Avodart® 0.5 mg softgel
PA
Dutasteride 0.5 mg-Tamsulosin 0.4 mg capsule
Jalyn® 0.5-0.4 mg capsule
PA
Silodosin 4 mg capsule
Rapaflo® 4 mg capsule
PA
Silodosin 8 mg capsule
Rapaflo® 8 mg capsule
PA
*TRADE NAMES ARE FOR REFERENCE ONLY
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Benzodiazepine Oral Solid Dosage Forms
(Implementation Date 12/07/2010)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria

Up to 124 units of any solid oral benzodiazepines paid by Medicaid per the
previous 31 calendar days.
Exemption from accumulation quantity limit



Diastat AcuDial rectal gel
Benzodiazepine injectable agents
Benzodiazepine oral liquid agents.
Additional criteria





Daily quantity limits apply for Alprazolam ER, Clobazam, Estazolam,
Flurazepam, Quazepam, Temazepam
Onfi tablet requires a Manual PA (See Clobazam [Onfi] Tablet)
Temazepam 22.5 mg Capsule requires a Manual PA (see Temazepam
22.5 mg)
Alprazolam XR [Xanax XR] additional approval criteria:
o > 18 years of age, AND
o >/= 90 days of Alprazolam XR therapy in the past 120 days
Alprazolam oral-disintegrating tablet [Niravam]
o > 18 years of age, AND
o One of the following:
 Long Term Care
 NPO (Appendix A)
Denial criteria

Therapeutic duplication with alprazolam
Additional criteria

Quantity limits apply
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Benzodiazepine Oral Liquid Dosage Forms
(Implementation Date 12/07/2010)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria


</= 6 years of age, OR
NPO (Appendix A)
Additional criteria
Quantity limits apply
Exemption criteria
Midazolam 2 mg/ml Syrup
 Claims for 30 ml or less will pay at point-of-sale for any age.
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Beta Adrenergic Blocking Agents
(Implemented 10/17/2007)
Prescribers may request an override for nonpreferred drugs by calling the
UAMS College of Pharmacy Evidence-Based Prescription Drug Program
Help Desk at 1-866-250-2518 (toll-free) or 501-526-4200 (local).
Preferred agents



Atenolol (Tenormin)
Metoprolol tartrate (Lopressor)
Propranolol HCl immediate-release (Inderal)
Preferred agents with criteria



Bisoprolol fumarate (Zebeta)
Carvedilol tablet (Coreg)
Metoprolol succinate extended-release (Toprol XL)
Nonpreferred agents











Acebutolol HCl (Sectral)
Betaxolol HCl (Kerlone)
Carvedilol phosphate capsule (Coreg CR)
Labetalol HCl (Normodyne)
Nadolol (Corgard)
Nebivolol HCl (Bystolic)
Penbutolol sulfate (Levatol)
Pindolol (Visken)
Propranolol HCl extended-release capsule (Inderal LA)
Propranolol HCl solution (Hemangeol)
Timolol maleate (Blocadren)
Approval criteria for preferred agents with criteria

Bisoprolol fumarate (Zebeta), Carvedilol Tablet (Coreg), and Metoprolol
succinate extended-release (Toprol XL)
 Congestive heart failure (Appendix D)
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Inhaled Long-acting Beta2 Agonist and Corticosteroid
Combination
(Implemented 08/11/2009)
Prescribers may request an override for nonpreferred drugs by calling the
UAMS College of Pharmacy Evidence-Based Prescription Drug Program
Help Desk at 1-866-250-2518 (toll-free) or 501-526-4200 (local).
Preferred agents with criteria


Budesonide/Formoterol fumarate dihydride inhalation aerosol
(Symbicort®)
Mometasone furoate/Formoterol fumarate dihydride Inhalation Aerosol
(Dulera®)
Approval criteria for preferred agents with criteria
Criterion 1: COPD diagnosis (Appendix G) in the past two years AND ≥ 18
years old AND ≥3 claims in the last 120 days of any product including:
Arcapta®, Anoro™ Ellipta®, Breo® Ellipta®, Brovana®, Foradil®,
Perforomist®, Serevent®, Spriva®, or Tudorza® Pressair®
OR
Criterion 2: Paid drug claim in drug history for Advair Diskus®, Advair®
HFA, Dulera®, or Symbicort® in the last six months
OR
Criterion 3: One of the following criteria below:
 > Three inhaled corticosteroid claims in the last 120 days,
OR
 > Three oral steroid claims in the last 120 days, OR
 Combination for > three claims (as defined below) in the last
120 days:
 One Inhaled Corticosteroid + 2 Oral Steroids
 Two Inhaled Corticosteroids + 1 Oral Steroids
Non-Preferred agents




Fluticasone furoate/Vilanterol inhalation powder (Breo® Ellipta®)
Fluticasone propionate/Salmeterol inhalation aerosol (Advair® HFA)
Fluticasone propionate/Salmeterol 250-50 MCG inhalation powder (Advair
250-50 Diskus®)
Fluticasone propionate/Salmeterol 500-50 MCG inhalation powder (Advair
500-50 Diskus®)
Nonpreferred agents with criteria

Fluticasone propionate/Salmeterol 100-50 MCG inhalation powder (Advair
100-50 Diskus®)
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Approval criteria for nonpreferred agents with criteria
Criterion 1: Beneficiary is between 4 years through 11 years of age AND
has a paid claim in drug history for Advair Diskus®, Advair® HFA,
Dulera®, or Symbicort® in the last six months
OR
Criterion 2: Beneficiary is between 4 years through 11 years of age AND
One of the following criteria below:
 > Three inhaled corticosteroid claims in the last 120 days,
OR
 > Three oral steroid claims in the last 120 days, OR
 Combination for > three claims (as defined below) in the last
120 days:
 One Inhaled Corticosteroid + 2 Oral Steroids
 Two Inhaled Corticosteroids + 1 Oral Steroids
Denial criteria


Absence of approval criteria
Therapeutic duplication between different Inhaled Long-acting Beta2
Agonists-Corticosteroid Combination Products
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Bexarotene Gel (Targretin)
(Implemented 10/01/2004)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Targretin
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Bosutinib (Bosulif 100mg and 500mg Tablets)
(Implemented 03/19/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Bosulif
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Botulinum Toxin Type A and Onabotulinumtoxina
(Botox 100 unit and 200 unit)
(Implementation Date 06/21/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Denial criteria


Diagnosis in Medicaid History of migraine headaches in the past 2 years, OR
At least one paid claim for Triptan medication in the past 2 years
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Bowel Prep Agents and Kits
(Implementation Date 10/11/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that do not require prior authorization












Colyte Solution
Colyte with Flavor Packets
Gavilyte-C Solution
Gavilyte-G Soution
Gavilyte-N Solution
Golytely Packet
Golytely Solution
Moviprep Powder Kit
Nulytely with Flavor Packs Solution
PEG-3350 and Electrolytes Solution
PEG-3350 with Flavor Packs Solution
Trilyte with Flavor Packets
Drugs that require manual review for prior authorization





Halflytely-Bisacodyl Bowel Kit
Osmoprep Tablet
Prepopik Powder Packet
Suclear Bowel Prep Kit
Suprep Bowel Prep Kit
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Bronchodilators, Long-Acting
(Implemented 08/11/2009)
Prescribers may request an override for nonpreferred drugs by calling the
UAMS College of Pharmacy Evidence-Based Prescription Drug Program
Help Desk at 1-866-250-2518 (toll-free) or 501-526-4200 (local).
Nonpreferred agents with criteria


Aclidinium bromide inhaler (Tudorza Pressair) (Click for Tudorza Critiera)
Tiotropium bromide inhaler (Spiriva Handihaler) (Click for Spiriva Criteria)
Nonpreferred agents without criteria







Arformoterol tartrate inhalation solution (Brovana)
Formoterol fumarate inhaler (Foradil)
Formoterol fumarate inhalation solution (Perforomist)
Indacaterol maleate inhaler (Arcapta Neohaler)
Salmeterol xiafoate disk with device (Serevent Diskus)
Umeclidinium bromide inhaler (Incruse Ellipta)
Umeclidinium-Vilanterol inhaler (Anoro Ellipta)
Approval criteria for nonpreferred agents with criteria

COPD (Appendix G)
Additional criteria
Quantity limits apply
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Bronchodilators, Short-Acting
(Implemented 08/11/2009)
Prescribers may request an override for nonpreferred drugs by calling the
UAMS College of Pharmacy Evidence-Based Prescription Drug Program
Help Desk at 1-866-250-2518 (toll-free) or 501-526-4200 (local).
Preferred agents



Albuterol sulfate 5mg/ml solution
Albuterol sulfate 0.83mg/ml solution
Albuterol sulfate HFA inhaler (Ventolin HFA 18 GRAM)
Nonpreferred agents









Albuterol 2.5mg/0.5ml solution
Albuterol sulfate 0.21mg/ml, 0.42mg/ml solution (Accuneb)
Albuterol sulfate HFA inhaler (ProAir HFA)
Albuterol sulfate HFA inhaler (Proventil HFA)
Albuterol sulfate HFA inhaler (Ventolin HFA 8 GRAM)
Levalbuterol HCl inhalation solution (Xopenex)
Levalbuterol tartrate HFA inhaler (Xopenex HFA)
Metaproterenol inhaler and solution (Alupent)
Pirbuterol acetate inhaler (Maxair Autohaler)
Nonpreferred agents with criteria


Albuterol sulfate-Ipratropium bromide inhaler(Combivent, Combivent
Respimat, Duoneb)
Ipratropium bromide HFA inhaler (Atrovent HFA)
Approval criteria for nonpreferred agents with criteria
One of the following diagnoses or procedures:
 Anoxic brain injury (348.1)
 COPD (Appendix G)
 Heart transplant (V421)
 Quadriplegic cerebral palsy (343.2)
 Respiratory insufficiency
 518.82 — Other pulmonary insufficiency, not elsewhere classified
 518.83 — Chronic respiratory failure
 518.84 — Acute and chronic respiratory failure
 Tracheostomy (Appendix B)
 Trachoemalacia congenital (748.3)
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Budesonide Extended-Release 9mg (Uceris)
(Implemented 07/09/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria

Submitted Diagnosis of Ulcerative Colitis in the past 2 years
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Budesonide EC 3mg Capsule (Entocort EC)
(Implemented 07/09/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria

Submitted Diagnosis of Crohn’s Disease in the past 2 years
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Buprenorphine (Subutex)
(Implemented 04/21/2009)
Prescribers are required to fax a letter of medical necessity and include all
supporting documentation for manual review to 501-683-4124.
Drugs that require manual review for prior authorization

Subutex
Additional criteria
Quantity limits apply
Link to Subutex statement of necessity—Microsoft Word format (.doc)
Link to Subutex statement of necessity—Portable Document Format (.pdf)
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Buprenorphine-Naloxone (Suboxone)
(Implemented 04/21/2009)
Prescribers are required to fax a letter of medical necessity and include all
supporting documentation for manual review to 501-683-4124.
Drugs that require manual review for prior authorization

Suboxone
Additional criteria
Quantity limits apply
Link to Suboxone statement of necessity—Microsoft Word format (.doc)
Link to Suboxone statement of necessity—Portable Document Format (.pdf)
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Butalbital Products
(Implemented 01/18/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that do not require a manual PA


Butalbital-Acetaminophen 50-325 mg TABLET (Marten-Tab)
Butalbital-Acetaminophen-Caffeine 50-325-40 mg TABLET (Esgic Tablet)
Drugs that require a manual PA


Butalbital-Acetaminophen 50-300 mg TABLET (Bupap 50-300 mg Tablet)
Butalbital-Acetaminophen-Caffeine 50-300-40 mg CAPSULE (Fioricet
Capsule)
Butalbital-Acetaminophen-Caffeine 50-325-40 mg CAPSULE (Esgic
Capsule)
Butalbital-Aspirin-Caffeine 50-325-40 mg CAPSULE (Fiorinal Capsule)


Age Edit
Recipient must be at least 12 Years of Age or greater
Quantity Edit




Solid Oral dosage forms of butalbital products will be limited up to a
maximum of 6 units per day
Solid Oral dosage forms of butalbital products will have a cumulative
quantity limit of 124 units per 31 days’ supply
The butalibital products that contain 750mg acetaminophen per unit will be
limited to a maximum of 5 units per day based on the maximum amount of
acetaminophen allowed per day
Oral liquid forms of butalbital will be limited to 60ml per day or up to 240ml
per prescription
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
C1 Esterase Inhibitor (Cinryze)
(Implemented 01/21/2011)
Prescribers are required to fax a letter of medical necessity and include all
supporting documentation for manual review to 501-683-4124.
Drugs that require manual review for prior authorization

Cinryze
A letter of medical necessity must be sent, along with ALL necessary
documentation substantiating ALL of the criteria listed below.
1.
Documented diagnosis of hereditary angioedema by an immunologist
AND
2.
The recipient’s history of HAE attacks is consistent with two or more
abdominal or respiratory attacks per month that require hospital ER intervention
with usage of Berinert® or Kalbitor® in the previous 6 consecutive months (ER
documentation is required)
AND
3.
The Member is NOT concurrently taking an angiotensin converting
enzyme (ACE) inhibitor or estrogen replacement therapy
AND
4.
The recipient has had an insufficient response or contraindication to
BOTH of the following classes of medication:
a. 17α – alkylated androgens (e.g. danazol, stanozolol, oxandrolone,
methyltestosterone)
b. Antifibrinolytic agents (e.g. ε – aminocaproic acid, tranexamic acid)
Note:
The Arkansas Medicaid Medical Director will work with hospital emergency
departments to ensure the availability of Berinert®, Kalbitor®, or Ruconest® for
acute attacks of HAE for authorized recipients.
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Cabozantinib Capsule (Cometriq)
(Implemented 07/09/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Cometriq
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Calcitrol (Vectical), Calcipotriene (Dovonex, Sorilux)
(Implemented 06/19/2006)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drug
Dovonex
Sorilux
Vectical
Approval criteria (New Start)
 Diagnosis of psoriasis in Medicaid history in previous 365 days,
AND
 2 paid claims of a topical corticosteroid in previous 27-60 days,
AND
 At least one paid claim for a topical corticosteroid must be from the very
high potency category.
Approval criteria (Continuation Criteria)
 Diagnosis of psoriasis in Medicaid history in previous 365 days,
AND
 The incoming claim matches claim in history in the previous 45 days,
AND
 At least two claims of a topical corticosteroid in previous 60 days in drug
claim history with at least one topical corticosteroid claim 14-60 days back
in history.
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Calcipotriene and Betamethasone Dipropionate
(Taclonex)
(Implemented 01/09/2008)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria



≥ 18 years of age, AND
History of three paid claims in the past 90 days for Calcipotriene
(Dovonex), AND
History of three paid claims in the past 90 days for a topical steroid
Denial criteria



< 18 years of age
Concurrent use of a topical corticosteroid
Failure to meet the approval criteria
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Calcitonin-salmon Nasal Spray (Miacalcin or Fortical)
(Implemented 08/17/2010)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria


For Males:
Diagnosis osteoporosis in the previous 2 years, AND





Diagnosis of esophageal strictures in the previous 2 years , OR
Diagnosis of esophageal achalasia in the previous 2 years
For Females:
Diagnosis of Postmenopause in the previous 2 years, AND
Diagnosis Osteoporosis in the previous 2 years, AND


Diagnosis of esophageal strictures in the previous 2 years , OR
Diagnosis of esophageal achalasia in the previous 2 years
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Calcitonin-salmon Injection (Miacalcin)
(Implemented 08/17/2010)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria

Diagnosis of hypercalcemia in the past two years.
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Calcium Channel Blockers
(Implemented 07/12/2005)
Prescribers may request an override for nonpreferred drugs by calling the
UAMS College of Pharmacy Evidence-Based Prescription Drug Program
Help Desk at 1-866-250-2518 (toll-free) or 501-526-4200 (local).
Preferred agents








Amlodipine besylate (Norvasc)
Amlodipine besylate/Olmesartan medoxomil* (Azor)
Amlodipine besylate/Olmesartan medoxomil/Hydrochlorothiazide*
(Tribenzor)
Amlodipine besylate/Valsartan* (Exforge)
Amlodipine besylate/Valsartan/Hydrocholorothiazide* (Exforge HCT)
Diltiazem HCl extended-release 120mg, 180mg, 240mg capsule (Dilacor
XR)
Nifedipine extended-release (Adalat CC, Procardia XL)
Verapamil extended-release tablet (Calan SR)
Nonpreferred agents









Amlodipine besylate/Atorvastatin calcium (Caduet)
Diltiazem HCl extended-release, CD, LA, SA, XR, XT (Cardizem, Tiazac)
Felodipine extended-release (Plendil)
Isradipine (Dynacirc)
Isradipine extended-release (Dynacirc CR)
Nicardipine HCl (Cardene)
Nicardipine HCL extended-release (Cardene SR)
Nisoldipine extended-release (Sular ER)
Verapamil extended-release capsule (Verelan)
*See Angiotensin II Receptor Antagonist criteria
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Carbidopa (Lodosyn)
(Implemented 01/12/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria

At least 1 paid Medicaid claim for Sinemet (carbidopa/levodopa) in the
previous 60 days, OR

At least 1 paid Medicaid claim for Stalevo in the previous 60 days.
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Carbidopa-Levodopa-Entacapone (Stalevo)
(Implemented 01/12/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria

No therapeutic duplication with Comtan.
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Cephalexin 750mg Capsule (Keflex)
(Implemented 07/09/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Keflex 750mg capsule
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Cephalosporins – 3rd Generation
(Implementation Date 3/18/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that do not require prior authorization







CEFDINIR 300 MG ORAL CAPSULE [OMNICEF]
CEFDINIR 125 MG/5 ML ORAL SUSPENSION [OMNICEF]
CEFDINIR 250 MG/5 ML ORAL SUSPENSION [OMNICEF
CEFPODOXIME PROXETIL 50 MG/ML ORAL SUSPENSION [VANTIN]
CEFPODOXIME PROXETIL100 MG/ML ORAL SUSPENSION [VANTIN]
CEFPODOXIME PROXETIL 100 MG ORAL TABLET [VANTIN]
CEFPODOXIME PROXETIL 200 MG ORAL TABLET [VANTIN]
Drugs that require manual review for prior authorization











CEFDITOREN PIVOXIL 200 MG ORAL TABLET [SPECTRACEF]*
CEFDITOREN PIVOXIL 400 MG ORAL TABLET [SPECTRACEF]*
CEFIXIME 400 MG ORAL CAPSULE [SUPRAX]
CEFIXIME 100 MG ORAL CHEWABLE TABLET [SUPRAX]
CEFIXIME 200 MG ORAL CHEWABLE TABLET [SUPRAX]
CEFIXIME 100 MG/5 ML ORAL SUSPENSION [SUPRAX]
CEFIXIME 200 MG/5 ML ORAL SUSPENSION [SUPRAX]
CEFIXIME 500 MG/5 ML ORAL SUSPENSION [SUPRAX]
CEFIXIME 400 MG ORAL TABLET [SUPRAX]
CEFTIBUTEN DIHYDRATE 400 MG ORAL CAPSULE [CEDAX]
CEFTIBUTEN DIHYDRATE 180 MG/5 ML ORAL SUSPENSION [CEDAX]
*Being removed from market. Limited availability.
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Ceritinib Capsule (Zykadia)
(Implemented 09/23/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Zykadia
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Chlorpheniramine ER 12mg
(Implemented 04/08/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria

>/= 90 days of Chlorpheniramine ER therapy in the past 120 days
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Ciclopirox 8% Topical Solution
(Implemented 01/13/2015)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that do not require prior authorization


Itraconazole Capsule [Sporanox]
Terbinafine Tablet [Lamisil]
Drugs that require manual PA



Ciclopirox 8% Topical Solution [Penlac]
Efinaconazole 10% Topical Solution [Jublia]
Tavaborole 5% Topical Solution [Kerydin]
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Cidofovir Injection (Vistide)
(Implemented 04/17/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Vistide
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Clobazam (Onfi)
(Implemented 07/09/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization


Onfi suspension
Onfi tablet
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Clonazepam Orally Disintegrating Tablet
(Implemented 10/11/2005)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria



< 6 years of age, OR
NPO (Appendix A), OR
Long Term Care Eligible
Approval criteria

Up to 124 Units of any solid oral benzodiazepines paid by Medicaid per
the previous 31 calendar days.
Exemption from accumulation quantity limit



Diastat AcuDial rectal gel
Benzodiazepine injectable agents
Benzodiazepine oral liquid agents.
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Clonidine and Guanfacine
(Implemented 07/11/2009)
Prescribers may request an override by calling the UAMS College of Pharmacy
Evidence-Based Prescription Drug Program Help Desk at 1-866-250-2518 (toll-free)
or 501-526-4200 (local).
Approval criteria
Patients ≥ 18 years of age
 All claims are approved
Patients < 18 years of age
 One therapeutic duplication with > 25% remaining on the last fill on
different dates of service allowed per 93 days between two clonidine
claims, two guanfacine claims, or one clonidine claim and one guanfacine
claim
 Cumulative quantity edits will apply (Table 3)
 Maximum daily dose edits will apply (Table 3.1)
Table 3 – Cumulative quantity edits
Generic name
Clonidine HCL 0.1mg tablet
Clonidine HCL 0.2mg tablet
Clonidine HCL 0.3mg tablet
Guanfacine 1mg tablet
Guanfacine 2mg tablet
Cumulative qty < 18 y/o
124 per 31 days
62 per 31 days
31 per 31 days
93 per 31 days
62 per 31 days
Table 3.1 – Maximum daily dose edits
Generic name
Clonidine HCL 0.1mg tablet
Clonidine HCL 0.2mg tablet
Clonidine HCL 0.3mg tablet
Guanfacine 1mg tablet
Guanfacine 2mg tablet
Link to Memorandum
Top of the document
Dose < 18 y/o
4 tabs per day
2 tabs per day
1 tab per day
3 tabs per day
2 tabs per day
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Clonidine Vials
(Implemented 07/08/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization


Clonidine HCl PF vials 5000mcg/10ml
Clonidine HCl PF vials 1000mcg/10ml
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Colchicine Tablet (Colcrys)
(Implemented 08/17/2010)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria


Diagnosis of gout in the past three years.
Diagnosis of Familial Mediterranean Fever (FMF)
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
COPD Agents
(Implemented 09/23/2014)
Prescribers may request an override for nonpreferred drugs by calling the
UAMS College of Pharmacy Evidence-Based Prescription Drug Program
Help Desk at 1-866-250-2518 (toll-free) or 501-526-4200 (local).
Nonpreferred agents

Roflumilast (Daliresp)
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Corticosteroids, Nasal Inhaled
(Implemented 11/28/2006)
Prescribers may request an override for nonpreferred drugs by calling the
UAMS College of Pharmacy Evidence-Based Prescription Drug Program
Help Desk at 1-866-250-2518 (toll-free) or 501-526-4200 (local).
Preferred agents

Fluticasone propionate nasal spray (Flonase)
Nonpreferred agents






Azelastine/fluticasone nasal spray (Dymista)
Beclomethasone dipropionate AQ nasal spray (Beconase AQ)
Beclomethasone dipropionate nasal spray (Qnasl)
Budesonide nasal spray (Rhinocort Aqua)
Ciclesonide nasal spray (Omnaris, Zetonna))
Triamcinolone acetonide AQ nasal spray (Nasacort AQ)
Nonpreferred agents with criteria


Fluticasone furoate nasal spray (Veramyst)
Mometasone furoate nasal spray (Nasonex)
Approval criteria for nonpreferred agents with criteria

Approvable if the beneficiary is between 2 years through 3 years of age
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Corticosteroids, Oral Inhaled
(Implemented 08/11/2009)
Prescribers may request an override for nonpreferred drugs by calling the
UAMS College of Pharmacy Evidence-Based Prescription Drug Program
Help Desk at 1-866-250-2518 (toll-free) or 501-526-4200 (local).
Preferred agents with criteria




Budesonide inhaler (Pulmicort Flexhaler)
Flunisolide inhaler (Aerospan)
Fluticasone propionate disk with device (Flovent Diskus)
Fluticasone proprionate HFA inhaler (Flovent HFA Inhaler)
Nonpreferred agents






Beclomethasone dipropionate inhaler (QVAR 7.3 gram)
Beclomethasone dipropionate inhaler (QVAR 8.7 gram)
Ciclesonide inhaler (Alvesco)
Fluticasone furoate inhaler (Arnuity Ellipta)
Mometasone furoate inhaler (Asmanex Twisthaler)
Triamcinolone acetonide inhaler (Azmacort)
Nonpreferred agents with criteria

Budesonide ampules for nebulizer (Pulmicort Respules)
Approval criteria for preferred agents with criteria
For beneficiaries ≥ 18 years old, if there is a diagnosis for COPD (Appendix G) in
the past two years, then it requires ≥ 3 claims in the past 120 days of any product
including : Arcapta®, Anoro™ Ellipta®, Breo® Ellipta®, Brovana®, Foradil®,
Perforomist®, Serevent®, Spiriva®, or Tudorza® Pressair® for approval.
Approval criteria for nonpreferred agents with criteria
Budesonide ampules for nebulizer
 < 4 years of age
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Corticotropin Gel Injection (Acthar HP)
(Implemented 07/09/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Acthar HP Gel Injection
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Crizotinib Capsule (Xalkori)
(Implemented 04/17/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization
Xalkori
Information required for the manual review process
Detection of ALK-positive NSCLC using an FDA-approved test, indicated for this
use
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Crofelemer Delayed Release Tablet (Fulyzaq)
(Implemented 07/09/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Fulyzaq
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Cromolyn Sodium Oral Solution (Gastrocrom)
(Implemented 09/21/2009)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria

Diagnosis of mastocytosis (congenital pigmentary anomalies or malignant
mast cell tumors) in the past three years
Additional criteria
Age edit : Approve > 2 years of age
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Crotamiton Cream and Lotion (Eurax)
(Implemented 01/12/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Eurax cream and lotion
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Cyclosporine 0.05% Eye Emulsion (Restasis)
(Implemented 01/18/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
Diagnosis of one of the following diagnoses associated with dry eye in the past
two years:
 Keratoconjunctivits sicca, non-Sjogren’s syndrome
 Keratoconjunctivits sicca, Sjogren’s syndrome
 Keratoconjunctivitis, exposure
 Tear film insufficiency, unspecified (Dry eye syndrome)
 Xerosis
Denial criteria
Therapeutic duplication with Lacrisert (hydroxypropyl cellulose)
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Cyproheptadine 4mg/10ml U.D. Cup
(Implemented 04/08/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
Currently LTC
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Cysteamine 0.44% Ophthalmic Drop (Cystaran)
(Implemented 12/10/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Cystaran Ophthalmic Drop
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Cysteamine DR Capsule (Procysbi)
(Implemented 03/18/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization


Procysbi 25mg DR Capsule
Procysbi 75mg DR Capsule
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Dabigatran Etexilate Mesylate Capsules (Pradaxa)
(Implemented 04/17/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria

Diagnosis of atrial fibrillation in Medicaid history in past 2 years, AND

No Therapeutic duplication allowed between different strengths of
Pradaxa®;

One (1) therapeutic duplication with overlapping days’ supply will be
allowed once per 186 days for inferred change in therapy between an
Pradaxa® claim and any of the following: a Xarelto® claim, a warfarin
claim, OR a Eliquis® claim, AND

The Pradaxa® claim and the warfarin claim, the Xarelto® claim, or the
Eliquis® claim cannot have the same date of service.
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Dalfampridine Extended-Release Tablet (Ampyra ER)
(Implemented 09/28/2010)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Ampyra ER 10mg tablet
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Dabrafenib (Tafinlar) Capsules
(Implemented 09/18/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Tafinlar
Additional Criteria

Quantity Limits Apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Dasatinib (Sprycel)
(Implemented 01/13/2015)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual PA

Sprycel
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Deferiprone Tablet (Ferriprox)
(Implemented 07/09/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Ferriprox tablet
Link to Memorandum
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Denosumab Syringe (Prolia)
(Implemented 01/13/2015)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Prolia
Prolia® will continue to be covered through a manual review PA on a case-bycase basis for the initial dose. POS PA continuation approval criteria for Prolia®
will apply as follows:
 1 Prolia® claim is found in Medicaid drug history in the previous 12
months.
 In addition, a therapeutic duplication edit will reject an incoming Prolia®
claim if an Xgeva® (denosumab) claim is found in the medical claims
history in previous 6 months.
 A quantity edit for Prolia® of 1 injection per 175 days will be implemented.
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Desmopressin (DDAVP) Nasal Spray and Solution
(Implemented 03/26/2008)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
Diagnosis in medicaid history of diabetes insipidus in the past three years.
Denial criteria


Diagnosis in medicaid history of nocturnal enuresis in the past three years.
Diagnosis in medicaid history of urinary incontinence in the past three
years.
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Dexamethasone Dose Pak (Dexpak and Zema-Pak)
(Implemented 10/11/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that do not require prior authorization

Dexamethasone 1.5mg Tablet
Drugs that require manual review for prior authorization


Dexpak
Zema-Pak
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Dextromethorphan HBr/Quinidine Capsule (Nuedexta)
(Implemented 06/21/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Nuedexta capsule
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Dihydroergotamine Mesylate Nasal Spray (Migranal)
(Implemented 07/09/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Migranal Nasal Spray
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Direct Renin Inhibitors
(Implemented 08/17/2010)
Prescribers may request an override for nonpreferred drugs by calling the
UAMS College of Pharmacy Evidence-Based Prescription Drug Program
Help Desk at 1-866-250-2518 (toll-free) or 501-526-4200 (local).
Preferred agents with criteria



Aliskiren (Tekturna)
Aliskiren/HCTZ (Tekturna HCT)
Aliskiren/Valsartan (Valturna)
Nonpreferred agents


Aliskiren/Amlodipine (Tekamlo)
Aliskiren/Amlodipine (Amturnide)
Approval criteria for preferred agent with criteria
New starts will require a paid claim in history of an ACE-Inhibitor product (ACEInhibitor, ACE-Inhibitor/HCTZ, or ACE-Inhibitor/Calcium Channel Blocker) in the
previous 27-45 days
OR
Continuation of therapy will require at least one paid claim in history of a
“Preferred with criteria” angiotensin receptor blocker or direct renin inhibitor in the
past 60 days
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Disopyramide CR (Norpace CR)
(Implemented 04/08/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria

>/= 90 days of Disopyramide CR therapy in the past 120 days
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Dornase Alfa inhalation Solution (Pulmozyme)
(Implemented 01/09/2008)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
Diagnosis of cystic fibrosis in medical history
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Dorzolamide-Timolol 2%-0.5% PF (Cosopt PF)
(Implemented 07/09/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that do not require prior authorization

Dorzolamide-Timolol 2%--0.5% (Cosopt)
Drugs that require manual review for prior authorization

Dorzolamide-Timolol 2%--0.5% preservative free (Cosopt PF)
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Doxepin 5% cream (Zonalon, Prudoxin)
(Implemented 09/21/2009)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
History of > two claims for a steroidal product (from very high, high, or moderate
strength) in the past 60 days
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Doxycycline/Minocycline
(Implemented 06/19/2008)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that do not require a manual PA
Generic MAC’d solid dosage forms of doxycycline and minocycline including:









Doxycycline hyclate 20 mg tablet (Periostat®)
Doxycycline hyclate 50 mg capsule (Vibramycin®)
Doxycycline hyclate 100 mg capsule (Vibramycin®)
Doxycycline hyclate 100 mg tablet (Vibra-tab®)
Doxycycline monohydrate 50 mg capsule (Monodox®)
Doxycycline monohydrate 100 mg capsule (Monodox®)
Minocycline HCl 50 mg capsule (Minocin®)
Minocycline HCl 75 mg capsule (Dynacin®)
Minocycline HCl 100 mg capsule (Minocin®)
Drugs that require manual PA












Doxycycline hyclate 75 mg delayed-release capsule & tablet (Doryx®)
Doxycycline hyclate 100 mg delayed-release capsule & tablet (Doryx®)
Doxycycline monohydrate 40 mg extended-release capsule (Oracea®)
Doxycycline monohydrate 75 mg capsule (Monodox®)
Doxycycline monohydrate 150 mg capsule (Adoxa®)
Doxycycline monohydrate 50 mg tablet (Adoxa®)
Doxycycline monohydrate 75 mg tablet (Adoxa®)
Doxycycline monohydrate 100 mg tablet (Adoxa®)
Doxycycline monohydrate 150 mg tablet (Adoxa®)
Minocycline HCl 50 mg tablet (Dynacin®)
Minocycline HCl 75 mg tablet (Dynacin®)
Minocycline HCl 100 mg tablet (Dynacin®)
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Doxylamine 5mg Chewable Tablet (Aldex AN)
(Implemented 09/28/2010)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
Patients </= 6 years of age that cannot swallow a solid oral dosage form.
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Doxylamine Succinate and Pyridoxine (Diclegis DR 1010)
(Implemented 09/18/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Diclegis
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Dronabinol (Marinol)
(Implemented 06/27/2007)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
Criterion 1:
 Age > 18 years of age, AND
 Submitted ICD-9 diagnosis HIV within the past 730 days, AND
 Submitted ICD-9 diagnosis for cachexia within the past 730 days, AND
 At least three paid drug claims in history identifying antiretrovirals (either
as single entity or combo drug) within the past 31 days, AND
 Paid claim for megestrol acetate (Megace) within the past 31 days (four
weeks) (Showing concomitant treatment)
Criterion 2:
 Age > 18 years of age, AND
 Submitted ICD-9 diagnosis HIV within the past 730 days, AND
 Submitted ICD-9 diagnosis for cachexia within the past 730 days , AND
 At least three paid drug claims in history identifying antiretrovirals (either
as single entity or combo drug) within the past 31 days.
Criterion 3:
 Age > 18 years of age, AND
 Submitted ICD-9 diagnosis malignant cancer within the past 365 days
AND
o Paid drug claim in history for antineoplastic agents within the past 45
days
OR
o Procedure code indicating radiation treatment within the past 45 days
AND
 Paid drug claim in history within the past 45 days for an oral 5-HT3
(serotonin) receptor antagonist, OR
 Paid drug claim in history within the past 45 days for a NK1 (neurokinin-1)
receptor antagonist
Denial criteria





Absence of approval criteria
Submitted ICD-9 diagnosis bipolar in medical history.
Submitted ICD-9 diagnosis depression in medical history.
Submitted ICD-9 diagnosis schizophrenia in medical history.
Submitted ICD-9 diagnosis substance or alcohol abuse in medical history.
Additional criteria
Quantity limits apply
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Droxidopa (Northera) Capsule
(Implemented 01/13/2015)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Northera
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Efinaconazole 10% Topical Solution (Jublia)
(Implemented 06/11/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that do not require prior authorization


Itraconazole Capsule [Sporanox]
Terbinafine Tablet [Lamisil]
Drugs that require manual PA



Ciclopirox 8% Topical Solution [Penlac]
Efinaconazole 10% Topical Solution [Jublia]
Tavaborole 5% Topical Solution [Kerydin]
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Eliglustat (Cerdelga) Capsule
(Implemented 01/13/2015)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual PA

Eliglustat (Cerdelga) Capsule
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Eltrombopag Olamine Tablet (Promacta)
(Implemented 07/09/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Promacta
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Emtricitabine (Emtriva)
(Implemented 01/12/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria for treatment of HIV-1 infection



A billed diagnosis of HIV/AIDS in the Medicaid history in previous 2
years; OR
Paid drug claim(s) in Medicaid history of other antiretroviral therapy
(ART), such as non-nucleoside reverse transcriptase inhibitors
(NNRTI), OR protease inhibitors (PI), OR integrase strand transfer
inhibitor (INSTI) in previous 6 months.
If there is no HIV/AIDS diagnosis in Medicaid history and no records of
other ART in the Medicaid drug profile, prescriber will be required to
follow the manual review process and submit documentation
confirming positive HIV diagnosis.
Denial criteria


Therapeutic duplication edit: paid claim within previous 30 days for
Truvada; OR
Absence of approval criteria.
Approval criteria for PrEp will require a manual review PA process
based upon the following:





Documentation from prescriber that patient is at high risk for acquiring
HIV infection; AND
Negative HIV test before starting and every 3 months thereafter; AND
Pregnancy test before starting and every 3 months thereafter. If
pregnant, provide documentation of patient understanding of potential
risks and benefits of using Truvada®, including contraindication with
breastfeeding; AND
Serum creatinine lab tests obtained prior to initiation, then every 6
months. Creatinine clearance should be >60 mL/min; AND
Documented testing for Hepatitis B Virus (HBV) and results submitted.
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Entacapone (Comtan)
(Implemented 01/12/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria

At least 1 paid Medicaid claim for Sinemet (carbidopa/levodopa) in the
past 60 days, AND

No therapeutic duplication with Stalevo.
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Entecavir (Baraclude)
(Implemented 09/24/2008)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria



No history of HIV/AIDS diagnosis in medical history, OR
HIV/AIDS diagnosis in medical history, AND
At least one paid Medicaid drug claim for antiretroviral in past 45 days
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Enzalutamide (Xtandi)
(Implemented 12/19/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Xtandi
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Eslicarbazepine (Aptiom)
(Implemented 07/08/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization




Aptiom 200 mg Tablet
Aptiom 400 mg Tablet
Aptiom 600 mg Tablet
Aptiom 800 mg Tablet
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Erythropoiesis stimulating agents
(Implemented 03/26/2008)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local)
Drugs that require manual PA



Darbepoetin alfa [Aranesp]
Epoetin alfa [Epogen]
Epoetin alfa [Procrit]
PA criteria
Prescriber must fax labwork with a recent hemoglobin level for approval
consideration. Fax documentation to 501-372-2971.
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Estrogen-replacement agents
(Implemented 07/11/2008)
Prescribers may request an override for nonpreferred drugs by calling the
UAMS College of Pharmacy Evidence-Based Prescription Drug Program
Help Desk at 1-866-250-2518 (toll-free) or 501-526-4200 (local).
Preferred agents


Estradiol 0.5mg, 1mg, 2mg oral tablet (Estrace)
Estropipate oral tablet (Ogen)
Nonpreferred agents











Estradiol acetate tablet (Femtrace)
Estradiol acetate vaginal ring (Femring)
Estradiol 1.5mg oral tablet (Estrace)
Estradiol spray (Evamist)
Estradiol topical gel (Divigel)
Estradiol transdermal (Alora, Climara)
Estradiol vaginal ring (Estring)
Estradiol vaginal tablet (Vagifem)
Estrogens, conjugated (Cenestin, Ejuvia, Premarin)
Estrogens, conjugated/Bazedoxifene (Duavee)
Estrogens, esterified (Menest)
Nonpreferred agents with criteria






Estradiol/drospirenone (Angeliq)
Estradiol/levonorgestrel (Climara Pro)
Estradiol/norethindrone (Activella)
Estradiol/norgestimate (Prefest)
Estrogens, conjugated/medroxyprogesterone (Premphase, Prempro)
Ethinyl estradiol/norethindrone acetate (Femhrt)
Approval criteria for nonpreferred agents with criteria
≥ 120 days of therapy in the previous 180 days for the same drug, strength, and
dosage form
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Everolimus Tablet (Afinitor)
(Implemented 07/23/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drug that requires a manual review for prior authorization

Afinitor
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Famotidine 40mg/5ml oral suspension (Pepcid)
(Implemented 09/24/2008)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria



At least two paid Medicaid drug claims for ranitidine syrup in the past 60
days, AND
≤ 6 years of age, OR
NPO (Appendix A)
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Febuxostat Tablet (Uloric)
(Implemented 07/09/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Uloric
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Fenofibrate and Fenofibric Acid Products
(Implemented 01/18/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that do not require prior authorization




FENOFIBRATE 54 MG ORAL TABLET [LOFIBRA]
FENOFIBRATE 67 MG ORAL CAPSULE [LOFIBRA]
FENOFIBRATE 160 MG ORAL TABLET [LOFIBRA]
GEMFIBROZIL 600 MG ORAL TABLET [LOPID]
Drugs that require manual review for prior authorization







ANTARA 30 MG, 43 MG, 90 MG, 130 MG ORAL CAPSULE (fenofibrate
micronized)
FIBRICOR 35 MG, 105 MG ORAL TABLET (fenofibric acid)
LIPOFEN 50 MG, 150 MG ORAL CAPSULE (fenofibrate)
LOFIBRA 134 MG, 200 MG ORAL CAPSULE (fenofibrate micronized)
TRICOR 48 MG, 145 MG ORAL TABLET (fenofibrate nanocrystallized)
TRIGLIDE 50 MG, 160 MG ORAL TABLET (fenofibrate nanocrystallized)
TRILIPIX DR 45 MG, 135 MG ORAL CAPSULE (fenofibric acid)
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Fentanyl Buccal Tablet (Fentora and Onsolis)
(Implemented 04/27/2005)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria



>/=18 years of age, AND
Opioid Tolerance of a ceiling dose for ≥ seven days during the past 30
days of one of the following: Fentanyl patch, Hydromorphone LA,
Morphine LA, or Oxycodone LA
AND
Cancer with malignancies as determined by:
o Diagnosis in past two years, OR
o Antineoplastic agents in the past 365 days
Denial criteria






< 18 years of age, OR
Remaining estimated days supply of fentanyl buccal tablet in history is >
25%
Thereapeutic duplication with Abstral
Therapeutic duplication with of Actiq
Therapeutic duplication with other strengths of Fentora
Therapeutic duplication with other strengths of Onsolis
Additional criteria
Quantity limits apply
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Fentanyl Nasal Spray (Lazanda)
(Implemented 09/23/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization


Lazanda 100mcg Nasal Spray
Lazanda 400mcg Nasal Spray
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Fentanyl 100mcg Sublingual Tablet (Abstral)
(Implemented 01/31/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria



>/=18 years of age, AND
Opioid Tolerance of a ceiling dose for ≥ seven days during the past 30
days of one of the following: Fentanyl patch, Hydromorphone LA,
Morphine LA, or Oxycodone LA
AND
Cancer with malignancies as determined by:
o Diagnosis in past two years, OR
o Antineoplastic agents in the past 365 days
Denial criteria






< 18 years of age, OR
Remaining estimated days supply of fentanyl buccal tablet in history is >
25%
Thereapeutic duplication with other strengths of Abstral
Therapeutic duplication with Actiq
Therapeutic duplication with Fentora
Therapeutic duplication with Onsolis
Additional criteria
Quantity limits apply
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Fentanyl Sublingual Spray (Subsys)
(Implemented 01/31/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria



>/=18 years of age, AND
Opioid Tolerance of a ceiling dose for ≥ seven days during the past 30
days of one of the following: Fentanyl patch, Hydromorphone LA,
Morphine LA, or Oxycodone LA
AND
Cancer with malignancies as determined by:
o Diagnosis in past two years, OR
o Antineoplastic agents in the past 365 days
Denial criteria






< 18 years of age, OR
Remaining estimated days supply of fentanyl sublingual spray in history is
> 25%
Thereapeutic duplication with Abstral
Therapeutic duplication with Actiq
Therapeutic duplication with Fentora
Therapeutic duplication with Onsolis
Additional criteria
Quantity limits apply
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Fentanyl citrate oral transmucosal (Actiq)
(Implemented 04/27/2005)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria



>/= 16 years of age, AND
Opioid tolerance of a ceiling dose for ≥ seven days during the past 30
days of one of the following: Fentanyl patch, Hydromorphone LA,
Morphine LA, or Oxycodone LA
AND
Cancer with malignancies as determined by:
o Diagnosis in past two years, OR
o Antineoplastic Agents in the past 365 days
Denial criteria






< 16 years of age, OR
Remaining estimated days supply of fentanyl citrate transmucosal in
history is > 25%
Therapeutic duplication with other strengths of Actiq
Therapeutic duplication with Fentora
Therapeutic duplication with Onsolis
Thereapeutic duplication with Abstral
Additional criteria
Quantity limits apply
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Fibromyalgia Agents
(Implemented 09/20/2011)
The non-preferred antiepileptic medications will be considered non-preferred for
treating fibromyalgia and neuropathic pain only. Medications listed as either
preferred or non-preferred status in this category may or may not include an FDA
approved indication for fibromyalgia or neuropathic pain. Use of these
medications for fibromyalgia, neuralgias, and neuropathic pain has been
reviewed through the evidence-based review process. Medications listed in this
category as either preferred or nonpreferred status are not to be construed as
endorsements for marketing of off-label use by the manufacturer or by Medicaid.
Prescribers may request an override for nonpreferred drugs by calling the
UAMS College of Pharmacy Evidence-Based Prescription Drug Program
Help Desk at 1-866-250-2518 (toll-free) or 501-526-4200 (local).
Preferred agents




Amitriptyline HCl (Elavil)
Cyclobenzaprine 10mg tablet (Flexeril)
Gabapentin 100mg, 300mg, 400mg capsule (Neurontin)
Nortriptyline HCl (Pamelor)
Preferred agents with criteria



Citalopram hydrobromide (Celexa) – see Second generation
antidepressant
Fluoxetine 10mg, 20mg capsule, 20mg/5ml solution (Prozac) – see
Second generation antidepressant
Paroxetine HCl immediate-release (Paxil) - Second generation
antidepressant
Nonpreferred agents with criteria:








Buproprion - all dosage forms (Aplenzin, Wellbutrin) – see Second
generation antidepressant
Carbamazepine - all dosage forms (Tegretol) – see Neuropathic pain
agents
Cyclobenzaprine 5mg, 7.5mg tablet, extended-release capsule (Amrix,
Fexmid, Flexeril) – see Skeletal muscle relaxants
Desipramine HCl (Norpramin)
Desvenlafaxine succinate (Pristiq) – see Second generation
antidepressant
Duloxetine HCl (Cymbalta) – see Second generation antidepressant
Escitalopram oxalate (Lexapro) – see Second generation antidepressant
Ethotoin (Peganone)
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria




















Fluoxetine HCl 10mg, 15mg, 20mg Tablet; 40mg capsule; and 90mg
weekly capsule (Prozac) – see Second generation antidepressant
Fluvoxamine maleate – all dosage forms (Luvox) – see Second generation
antidepressant
Gabapentin 250mg/5ml solution, 600mg, 800mg tablet – see Neuropathic
pain agents
Imipramine HCl and pamoate (Tofranil)
Lacosamide (Vimpat) – see Neuropathic pain agents
Lamotrigine (Lamictal) – see Neuropathic pain agents
Levetiracetam (Keppra)
Milnacipran HCl (Savella) – see Second generation antidepressant
Mirtazapine (Remeron) – see Second generation antidepressant
Nefazodone HCl (Serzone) – see Second generation antidepressant
Oxcarbazepine (Trileptal) – see Neuropathic pain agents
Paroxetine HCl controlled-release tablet, and 10mg/5ml suspension (Paxil
CR) – see Second generation antidepressant
Paroxetine mesylate (Pexeva) – see Second generation antidepressant
Phenytoin 100mg extended-release capsule (Dilantin)
Pregabalin (Lyrica) – see Neuropathic pain agents
Sertraline HCl (Zoloft) – see Second generation antidepressant
Tiagabine (Gabitril) –
Valproic Acid (Depakene, Stavzor) – see Neuropathic pain agents
Venlafaxine, all dosage forms (Effexor, Effexor XR) – see Second
generation antidepressant
Zonisamide (Zonegran)
Approval criteria for nonpreferred agents with criteria


No diagnosis of myalgia and myositis, unspecified (ICD-9 729.1) in the
past three years
Drugs with a link to neuropathic pain agents, second generation
antidepressants, or skeletal muscle relaxants have additional criteria to
meet for approval
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Fidaxomicin (Dificid)
(Implemented 01/12/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria


>/= 18 years of age, AND
At least 1 paid claim in Medicaid history for Vancomycin (oral or injectable
compounded for oral use) in the previous 10-30 days.
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Finasteride Tablet (Proscar)
(Implemented 07/09/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria

Diagnosis of Benign Prostatic Hypertrophy in the past 3 years
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Fluorouracil Solution/Cream (Efudex)
(Implemented 06/21/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval for Fluorouracil 2% Solution:
 Diagnosis of Actinic Keratosis in Medicaid history in the past 2 months,
AND
 No therapeutic duplication with Diclofenac Sodium 3% Gel [Solaraze], OR
 No therapeutic duplication with other strengths of Fluorouracil Cream or
Solution [Carac, Efudex, Fluoroplex], OR
 No therapeutic duplication with Imiquimod Cream [Aldara, Zyclara], OR
 No therapeutic duplication with Ingenol Gel [Picato]
Approval for Fluorouracil 5% Cream or Solution:
 Diagnosis of Actinic Keratosis or Basal Cell Carcinoma in Medicaid history
in the past 2 months AND
 No therapeutic duplication with Diclofenac Sodium 3% Gel [Solaraze], OR
 No therapeutic duplication with other strengths of Fluorouracil Cream or
Solution [Carac, Efudex, Fluoroplex], OR
 No therapeutic duplication with Imiquimod Cream [Aldara, Zyclara], OR
 No therapeutic duplication with Ingenol Gel [Picato]
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Fluorouracil Cream (Carac 0.5% and Fluoroplex 1%)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval for fluorouracil 0.5% and 1% Cream:
 Diagnosis of Actinic Keratosis in Medicaid history in the past 2 months,
AND
 No therapeutic duplication with Diclofenac Sodium 3% Gel [Solaraze], OR
 No therapeutic duplication with other strengths of Fluorouracil Cream or
Solution [Carac, Efudex, Fluoroplex], OR
 No therapeutic duplication with Imiquimod Cream [Aldara, Zyclara], OR
 No therapeutic duplication with Ingenol Gel [Picato]
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Fosamprenavir Calcium (Lexiva) Tablet
(Implemented 09/18/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval for Lexiva Tablet:

If the Medicaid recipient does not have a ritonavir claim in Medicaid history
in the previous 45 days, a maximum quantity of 4 tablets per day will be
allowed and a cumulative quantity of 124 tablets per 31 days.

If the Medicaid recipient does have a ritonavir claim in Medicaid history in
the previous 45 days, a maximum quantity of 2 tablets per day will be
allowed and a cumulative quantity of 62 per 31 days.
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Fosamprenavir Calcium (Lexiva) 50mg/5ml
Suspension
(Implemented 09/18/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval for Oral suspension 50 mg/5 ml:
 < 6 years of age
 NPO diagnosis in Medicaid history.
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Galantamine ER (Razadyne ER)
(Implemented 04/08/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria

>/= 90 days of Galantamine ER therapy in the past 120 days
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Galantamine Solution (Razadyne)
(Implemented 09/18/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval for Razadyne:
 Age > 50 years of age, AND
 Diagnosis of NPO in the Medicaid History
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Glycerol Phenylbutyrate Liquid (Ravicti)
(Implemented 07/09/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Ravicti
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Glycophos 20ml Vial
(Implemented 09/18/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Glycophos 20ml vial
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Glycopyrrolate 0.2 mg/ml vial
(Implemented 07/08/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that do not require prior authorization

Glycopyrrolate 1 mg/5 ml oral solution (Cuvposa)
Drugs that require manual review for prior authorization

Glycopyrrolate 0.2 mg/ml vial
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Glycopyrrolate 1.5mg Tablet (Glycate)
(Implemented 03/18/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drug that requires a manual review for prior authorization

Glycate 1.5mg
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Hemorrhoid Preparations
(Implemented 01/12/2010)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
History of at least three claims for three different products that do not require
prior authorization within the previous 60 days.
LABELER CODE
65649
68220
10631
64980
68220
Link to Memorandum
Top of the document
LABEL NAME
ANUSOL-HC 2.5% CREAM
PROCTOFOAM-HC 1%-1% FOAM
PROCTOSOL-HC 2.5% CREAM
PROCTOZONE-HC 2.5% CREAM
CORTIFOAM 10% AEROSOL
PA STATUS
No PA
No PA
No PA
No PA
PA
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Hepatitis C Medications
(Implemented 10/21/2009)
Prescribers are required to complete the HCV Statement of Medical
Necessity and fax to 501-683-4124.
Drugs that require a manual PA























Incivek 375 mg tablet
Infergen 9mcg/0.3mls
Infergen 15mcg/0.5mls
Olysio (Simeprevir)
Pegasys 180mcg (1 ml vial)
Pegasys 180mcg (1 kit) – four doses
Peg Intron 50mcg (1 kit)
Peg Intron 80mcg (1 kit)
Peg Intron 120mcg (1 kit)
Peg Intron 150mcg (1 kit)
Peg Intron 50mcg Redipen (1 kit)
Peg Intron 80mcg Redipen (1 kit)
Peg Intron 120mcg Redipen (1 kit)
Peg Intron 150mcg Redipen (1 kit)
Ribavirin 200mg capsule
Ribavirin 200mg tablet
Rebetol 40mg/ml solution
Ribasphere 400mg tablet
Ribasphere 600mg tablet
Ribapak 400-400mg dosepack
Ribapak 400-600mg dosepack
Sovaldi (Sofosbuvir)
Victrelis 200mg capsule
Link to Hepatitis C prior authorization form—Microsoft Word format (.doc)
Link to Hepatitis C prior authorization form—Portable Document Format (.pdf)
Link to Memorandum
Link to Memorandum
Link to Updated Criteria
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
HMG-CoA Reductase Inhibitors
(Implemented 06/10/2008)
Prescribers may request an override for nonpreferred drugs by calling the
UAMS College of Pharmacy Evidence-Based Prescription Drug Program
Help Desk at 1-866-250-2518 (toll-free) or 501-526-4200 (local).
Preferred agents



Atorvastatin calcium (Lipitor)
Pravastatin sodium (Pravachol)
Simvastatin 5mg, 10mg, 20mg, 40mg (Zocor)
Preferred agents with criteria

Simvastatin 80mg (Zocor)
Nonpreferred agents









Atorvastatin calcium/Ezetimibe (Liptruzet)
Fluvastatin sodium (Lescol)
Lovastatin (Mevacor)
Lovastatin/Niacin extended-release (Advicor)
Pitavastatin calclium (Livalo)
Rosuvastatin calcium (Crestor)
Simvastatin/Ezetimibe (Vytorin)
Simvastatin/Niacin (Simcor)
Simvastatin/Sitagliptin (Juvisync)
Approval criteria for agents with criteria
Simvastatin 80mg
 Ten or more claims for Sivastatin 80mg within past twelve months
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Hydrocodone ER Capsule (Zohydro ER)
(Implemented 07/08/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Zohydro ER
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Hydroxypropyl Cellulose 5mg Eye Insert (Lacrisert)
(Implemented 01/18/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
Diagnosis of one of the following diagnoses associated with dry eye in the past
two years:
 Keratoconjunctivits sicca, non-Sjogren’s syndrome
 Keratoconjunctivits sicca, Sjogren’s syndrome
 Keratoconjunctivitis, exposure
 Tear film insufficiency, unspecified (Dry eye syndrome)
 Xerosis
Denial criteria
Therapeutic duplication with Restasis (Cyclosporine)
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Ibrutinib (Imbruvica) Capsule
(Implemented 03/18/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drug that requires a manual review for prior authorization

Imbruvica 140mg Capsule
Additional Criteria

Quantity Limits Apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Icatibant (Firazyr)
(Implemented 01/12/2012)
Providers requesting a Prior Authorization (PA) should call the Medicaid
Pharmacy Program, 501-683-4120.
Drugs that require manual review for prior authorization

Firazyr
Additional criteria
 Quantity limits apply
 Age >17 years of Age
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Icosapent Ethyl Capsule (Vascepa)
(Implemented 07/09/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Vascepa
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Idelaisib (Zydelig) Tablet
(Implemented 01/13/2015)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Zydelig
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Imiquimod (Aldara)
(Implemented 06/27/2007)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria








> 12 years of age AND,
Submitted ICD-9 diagnosis for superficial basal cell carcinoma (sBCC)
within past two months, OR
Submitted ICD-9 diagnosis for actinic keratosis (AK) within past two
months, OR
Submitted ICD-9 diagnosis for Condyloma Acuminata (or commonly
known as external genital or perianal warts) within past two months, AND
No Therapeutic Duplication with Diclofenac Sodium 3% gel
No Therapeutic Duplication with Fluorouracil Cream/Solution Topical
No Therapeutic Duplication with other strengths of Imiquimod Cream
Topical
No Therapeutic Duplication with Ingenol gel Topical
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Imiquimod (Zyclara)
(Implemented 04/27/2010)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria







> 12 years of age, AND
Submitted ICD-9 diagnosis for actinic keratosis (AK) within past two
months, OR
Submitted ICD-9 diagnosis for Condyloma Acuminanta (commonly known
as external genital or perianal warts) within past two months, AND
No Therapeutic Duplication with Diclofenac Sodium 3% gel
No Therapeutic Duplication with Fluorouracil Cream/Solution Topical
No Therapeutic Duplication with other strengths of Imiquimod Cream
Topical
No Therapeutic Duplication with Ingenol gel Topical
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Immunologic Agents (Multiple Sclerosis)
(Implemented 09/27/2011)
Prescribers may request an override for nonpreferred drugs by calling the
UAMS College of Pharmacy Evidence-Based Prescription Drug Program
Help Desk at 1-866-250-2518 (toll-free) or 501-526-4200 (local).
Preferred agents


Glatiramer acetate 20 mg injection (Copaxone®)
Interferon Beta – 1A injection (Avonex®)
Non-Preferred agents








Dimethyl fumarate capsule (Tecfidera®)
Glatiramer acetate 40 mg injection (Copaxone®)
Fingolimod HCl capsule (Gilenya®)
Interferon Beta – 1A/albumin (Rebif®)
Interferon Beta – 1B injection (Betaseron®)
Interferon Beta – 1B kit (Extavia®)
Peginterferon Beta – 1A (Plegridy®)
Teriflunomide tablet (Aubagio®)
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Ingenol Mebutate (Picato Gel)
(Implemented 03/08/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria






>/= to 18 Years of Age
Submitted ICD-9 diagnosis for actinic keratosis (AK) within past two
months, AND
No Therapeutic Duplication with Diclofenac Sodium 3% gel
No Therapeutic Duplication with Fluorouracil Cream/Solution Topical
No Therapeutic Duplication with Imiquimod Cream Topical
No Therapeutic Duplication with other strengths of Ingenol gel Topical
Additional criteria
Quantity limits apply
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Insulin Pens
(Implemented 04/08/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria applies to all strengths of the following insulin
pens

















Apridra® (insulin glulisine)
Humalog® (insulin lispro)
Humalog® Mix 50-50
Humalog® Mix 75-25
Humulin® (insulin human) N
Humulin® R, Lantus® (insulin glargine)
Levemir® (insulin detemir)
Novolin® (human insulin) 70-30
Novolin® N
Novolin® R
NovoLog® (insulin aspart)
NovoLog® Mix 70-30
Relion Humulin® 70-30
Relion Humulin® N
Relion Humulin® R
Relion Novolin® 70-30
Relion Novolin® N
Approval criteria
Criterion 1
 ≤ 18 years of age, AND
 Not currently in LTC, AND
 Quantity </= 15 ml per 31-day supply.
Criterion 2
 ≤ 18 years of age, AND
 Currently in LTC, AND
 Medicaid paid claims for ≥ 90 days of the same insulin pen
formulation in the previous 120 days, AND
 Quantity </= 15 ml per 31-day supply.
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Criterion 3
 >18 years of age, AND
 Medicaid paid claims for ≥ 90 days of the same insulin pen
formulation in the previous 120 days.
Link to Memorandum
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Isosorbide Dinitrate/Hydralazine (BiDil)
(Implemented 09/18/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

BiDil
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Itraconazle (Onmel) 200mg Tablet
(Implemented 03/19/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Onmel
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Isotretinoin
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require a manual PA




Isotretinoin 10 mg (Amnesteem, Claravis)
Isotretinoin 20 mg (Amnesteem, Claravis, Sotret)
Isotretinoin 30 mg (Claravis)
Isotretinoin 40 mg (Amnesteem, Claravis)
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Itrazonazole Oral Solution (Sporanox)
(Implemented 10/11/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria



History of at least two claims for fluconazole (tablets or suspension) in the
previous 7-30 days, OR
One claim each of Nystatin Suspension and fluconazole (tablets or
suspension) in the previous 7-30 days, OR
NPO diagnosis in Medicaid history
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Ivacaftor Tablet (Kalydeco)
(Implemented 07/09/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Kalydeco
Link to Memorandum
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Ivermectin 0.5% Lotion (Sklice)
(Implemented 06/18/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Sklice 0.5% Lotion
Additional criteria
 Quantity limits apply
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Kits
(Implemented 08/17/2010)
All requests for “kits” or “combo pack” products (products that consist of
packaging multiple products under one NDC) require a manual review. The
underlined individual active ingredients (listed next to the product) do not require
a PA.
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require a manual PA














CICLODAN 0.77% CREAM KIT (CICLOPIROX 0.77% CREAM – HAIR &
BODY CLEANSER)
CICLOPIROX 8% KIT (CICLOPIROX 8% TOPICAL SOLUTION NAIL
LACQUER – VITAMIN E CAPSULES – LACQUER REMOVER)
CENTANY AT 2% OINMENT KIT (MUPIROCON 2% OINTMENT – STERILE
GAUZE – TAPE)
CNL 8 NAIL KIT (CICLOPIROX 8% TOPICAL SOLUTION NAIL LACQUER –
EMORY BOARD – LACQUER REMOVER)
HALONATE PAC COMBO PACK (HALOBETASOL PROPIONATE 0.5%
OINTMENT – AMMONIUM LACTATE 12% LOTION)
KETODAN 2% FOAM KIT (KETOCONAZOLE 2% TOPICAL FOAM – HAIR
& BODY CLEANSER)
LIDOCAINE-PRILOCAINE 2.5%-2.5% CREAM KIT (LIDOCAINPRILOCAINE 2.5%-2.5% CREAM – OCCLUSIVE DRESSINGS)
PEDIADERM AF KIT (NYSTATIN 100,000 UNITS/GRAM CREAM –
EMOLLIENT DIAPER CREAM)
PEDIADERM HC 2% KIT (HYDROCORTISONE 2% LOTION – EMOLLIENT
DIAPER CREAM)
PEDIADERM TA 0.1% KIT (TRIAMCINOLONE ACETONIDE 0.1% CREAM –
EMOLLIENT DIAPER CREAM)
PEDIPIROX-4 NAIL KIT (CICLOPIROX 8% TOPICAL SOLUTION NAIL
LACQUER – ALCOHOL NAIL LACQUER REMOVAL PADS)
ROSADAN 0.75% CREAM KIT (METRONIDAZOLE 0.75% CREAM –
MOISTURIZING SKIN WASH)
ROSADAN 0.75% GEL KIT (METRONIDAZOLE 0.75% GEL –
MOISTURIZING SKIN WASH)
ROWASA 4 GM/60 ML ENEMA KIT (MESALAMINE 4 GM/60 ML ENEMA –
CLEANSING WIPES)
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria






SYNALAR 0.025% CREAM KIT (FLUOCINOLONE ACETONIDE 0.025%
TOPICAL CREAM – EMOLLIENT CREAM)
SYNALAR 0.025% OINTMENT KIT (FLUOCINOLONE ACETONIDE 0.025%
TOPICAL OINTMENT – EMOLLIENT CREAM)
SYNAGLAR TS 0.01% KIT (FLUOCINOLONE ACETONIDE 0.01% TOPICAL
SOLUTION – HAIR & BODY CLEANSER)
TERBINEX KIT (TERBINAFINE HCL 250 ORAL TABLETS –
HYDROXYPROPYL-CHITOSAN 1% NAIL LACQUER)
ULTRAVATE X CREAM COMBO PACK (HALOBETASOL PROPIONATE
0.05% TOPICAL CREAM – AMMONIUM LACTATE 10% MOISTURIZING
CREAM)
ULTRAVATE X OINTMENT COMBO PACK (HALOBETASOL
PROPIONATE 0.05% TOPICAL OINTMENT – AMMONIUM LACTATE 10%
MOISTURIZING CREAM)
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Lamotrigine Kits (Lamictal Start and Patient Titration
Kits)
(Implemented 03/18/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that do not require prior authorization* if being used for
approved diagnosis

Lamotrigine Tablets*
Drugs that require manual review for prior authorization



Lamictal ODT Start Kit (Blue) contains 25mg and 50mg tablets
Lamictal ODT Start Kit (Green)contains 50mg and 100mg tablets
Lamictal ODT Start Kit (Orange)contains 25mg, 50mg, and 100mg tablets



Lamictal Tablet Start Kit (Blue) contains 25mg tablets
Lamictal Tablet Start Kit (Green) contains 25mg and 100mg tablets
Lamictal Tablet Start Kit (Orange) contains 25mg and 100mg tablets

Lamictal XR Start Kit (Blue) contains 25mg and 50mg extended-release
tablets
Lamictal XR Start Kit (Green) contains 50mg, 100mg, and 200mg
extended-release tablets
Lamictal XR Start Kit (Orange) contains 25mg, 50mg, and 100mg
extended-release tablets


Lamictal Start Kits are designed for titration during the first 5 weeks of therapy
and contain a single entity drug that typically does not require prior
authorization. Daily dosing instructions are determined by the patient’s current
antiepileptic regimen.
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Lansoprazole, Amoxicillin, and Clarithromycin
combination (Prevpac)
(Implemented 01/12/2005)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
Criterion 1:
 No history of lansoprazole, amoxicillin, and clarithromycin combination
(Prevpac) in the last 365 days, AND,
 No history of omeprazole, amoxicillin, and clarithromycin combination
(Prevpac) in the last 365 days, AND,
 No concurrent proton pump inhibitor therapy within the past 30 days.
Criterion 2:
 No history of lansoprazole, amoxicillin, and clarithromycin combination
(Prevpac) in the last 365 days, AND,
 No history of omeprazole, amoxicillin, and clarithromycin combination
(Prevpac) in the last 365 days, AND,
 No concurrent proton pump inhibitor therapy within the past 30 days.
Criterion 3:
 No history of metronidazole/tetracycline/bismuth combination (Helidac) in
the last 365 days, OR
 No history of metronidazole/tetracycline/bismuth combination (Pylera) in
the last 365 days.
Denial criteria
Criterion 1:
 History of lansoprazole, amoxicillin, and clarithromycin combination
(Prevpac) in the last 365 days, OR
 Current proton pump inhibitor therapy within the past 30 days
Criterion 2:
 No history of lansoprazole, amoxicillin, and clarithromycin combination
(Prevpac) in the last 365 days, AND,
 No history of omeprazole, amoxicillin, and clarithromycin combination
(Prevpac) in the last 365 days, AND,
 No concurrent proton pump inhibitor therapy within the past 30 days.
Criterion 3:
 No history of metronidazole/tetracycline/bismuth combination (Helidac) in
the last 365 days, OR
 No history of metronidazole/tetracycline/bismuth combination (Pylera) in
the last 365 days.
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Additional criteria
Quantity limits apply
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Leukotriene Receptor Antagonists
(Implemented 08/11/2009)
Prescribers may request an override for nonpreferred drugs by calling
the UAMS College of Pharmacy Evidence-Based Prescription Drug
Program Help Desk at 1-866-250-2518 (toll-free) or 501-526-4200 (local).
Preferred agent with criteria

Montelukast sodium (Singulair)
Nonpreferred agents


Zafirlukast (Accolate)
Zileuton (Zyflo)
Approval criteria for preferred agents
Criterion 1:
A. If a paid drug claim in history for an inhaled corticosteroid, long-acting
beta2 agonist/inhaled corticosteroid, or short-acting beta2 agonist in the
last 365 days, then
B. One of the following criteria below:
 < Two claims for short-acting beta2 in the last 365 days, AND
 < One claim for an oral corticosteroid in the last 183 days
OR
 IF the patient exceeds any of the above criteria, then the asthma patient
must have a claim for an inhaled asthma controller (ICS or ICS/LABA) in
Medicaid drug history in last 45 days.
OR
Criterion 2:
A. If no paid drug claim in history for an inhaled corticosteroid, long-acting
beta2 agonist/inhaled corticosteroid, or short-acting beta2 agonist in the
last 365 days, then
B. One of the following criteria below:
 > One claim for an inhaled nasal steroid from the 7th day to the124th day
in Medicaid history, OR
 > One claim for a second generation antihistamine from the 7th day to
the124th day in Medicaid history
OR
Criterion 3:
A. A diagnosis code for COPD (Appendix G) in patient history in the past
2 years AND patient is greater than 18 years old AND
B. One of the following criteria below:
 > One claim for an inhaled nasal steroid from the 7th day to the124th day
in Medicaid history, OR
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria

> One claim for a second generation antihistamine from the 7th day to
the124th day in Medicaid history
Denial criteria


Failure to meet approval criteria
Therapeutic duplication with a LTRA other than the one on the incoming
claim if >25% of the days supply of the claim in history remains
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Levetiracetam ER (Keppra ER)
(Implemented 04/08/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria

>/= 90 days of Levetiracetam ER therapy in the past 120 days
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Levofloxacin 500mg/20ml U.D. Cup
(Implemented 04/08/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
Currently LTC
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Levothyroxine Capsule (Tirosint)
(Implemented 08/17/2010)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that do not require prior authorization

All strengths of generic levothyroxine tablet
Drugs that require manual review for prior authorization

Tirosint Capsule
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Levothyroxine Vial
(Implemented 04/17/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Levothyroxine 200 mcg vial

Levothyroxine 500 mcg vial
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Lidocaine-Prilocaine 2.5%-2.5% Cream (Emla)
(Implemented 07/09/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Lithium ER or SA
(Implemented 04/08/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria

>/= 90 days of Lithium ER or Lithium SA therapy in the past 120 days
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Linacoltide (Linzess)
(Implemented 04/08/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
Criterion 1
 > 18 years of age, AND
 Paid drug claim for Linzess (Linacoltide) within the past 60 days,
Criterion 2:
 > 18 years of age, AND
 Paid claim for 30 day supply of polyethylene glycol 3350 (Miralax,
Glycolax) within previous 45 days, AND
Denial criteria




Absence of approval criteria
History of mechanical gastrointestinal obstruction
Age < 18 years of age
>/=1 Paid claim for an opioid in the past 60 days
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Lomitapide Mesylate Capsule (Juxtapid)
(Implemented 07/09/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Juxtapid
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Low Molecular Weight Heparins (Dalteparin [Fragmin],
Enoxaparin [Lovenox], Tinzaparin [Innohep])
(Implemented 04/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria


No Therapeutic Duplication with Xarelto 10mg, AND
No Therapeutic Duplication with other Low Molecular Weight Heparins
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Lindane
(Implemented 03/22/2006)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
Lindane Shampoo
 History of at least one permethrin or pyrethrin/piperonyl in the last 28 days
which can include a combination of any of the following:
o Two permethrin claims OR,
o Two pyrethrin-piperonyl claims OR,
o One permethrin and one pyrethrin-piperonyl claims, OR
o One permethrin claim and one malathion claim, OR,
o One pyrethrin-piperonyl claim and one malathion claim, AND
 Patient >/= 13 years old
Lindane Lotion
 History of at least one permethrin or pyrethrin-piperonyl in the last 28 days,
AND
 Patient >/= 13 years old
Denial criteria


Patient < 13 years of age, OR
Previous claim history of Lindane in the last 180 days
Additional criteria
Quantity limits apply
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Lubiprostone (Amitiza)
(Implemented 06/27/2007)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
Criterion 1:
 > 18 years of age, AND
 Paid drug claim for Amitiza (Lubiprostone) within the past 60 days
Criterion 2:
 > 18 years of age, AND
 Paid claim for 30 day supply of polyethylene glycol 3350 (Miralax,
Glycolax) within previous 45 days, AND
 Amitiza dose of one tablet per day
Denial criteria



Absence of approval criteria
History of mechanical gastrointestinal obstruction
Age < 18 years of age
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Leuprolied/Norethindrone (Lupaneta) 2.5-5mg 1 month
kit and 11.25-5mg 3 month kit
(Implemented 07/08/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria

Billed diagnosis of endometriosis or uterine leiomyoma (fibroids) AND

<12 billed claims of 3.75mg leuprolide injection (which would include
Lupaneta®) in the previous 3 year Medicaid history, OR

< 4 billed claims of 11.25mg leuprolide injection (which would include
Lupaneta®) in the previous 3 year Medicaid history, AND

No Therapeutic Duplication with other strengths of Lupron.
Denial Criterion
 Diagnosis of infertility in Medicaid history (3 year look back), OR
 Thrombophlebitis, OR
 Thromboembolic disorders, OR
 Cerebral apoplexy in Medicaid history; OR
 Carcinoma of the breast in Medicaid history.
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Lupron
(Implemented 06/21/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Lupron depot 11.25 mg 3 mo kit
Lupron depot 22.5 mg 3 mo kit
Lupron depot 3.75 mg kit
Lupron depot 7.5 mg kit
Lupron depot-4 month kit
Lupron depot-ped 11.25 mg kit
Lupron depot-ped 15 mg kit
Lupron depot-ped 7.5 mg kit
Criterion 1 for Lupron-Depot PED® 7.5 mg, 11.25 mg, and 15 mg:

Diagnosis of Central Precocious Puberty (CPP) in Medicaid History, AND

Girls <11 Years of Age or Boys <12 Years of Age, AND

Procedure code for CT scan of the head within last 2 years, AND

Procedure code in Medicaid History for Ultrasound of pelvic/adrenal/testicular
area within last 2 years, AND

Procedure code in Medicaid History for Bone Age study in the last 2 years,
AND

No Therapeutic Duplication with other strengths of Lupron.
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Criterion 2 for Lupron-Depot® 3.75 mg, and 11.25 mg-3 month
•
Billed diagnosis of endometriosis or uterine leiomyoma (fibroids) AND
•
<12 billed claims of 3.75mg leuprolide injection (which would include
Lupaneta®) in the previous 3 year Medicaid history, OR
•
< 4 billed claims of 11.25mg leuprolide injection (which would include
Lupaneta®) in the previous 3 year Medicaid history
AND

No Therapeutic Duplication with other strengths of Lupron.
Denial Criterion
 Diagnosis of infertility
Criterion 3 for Lupron-Depot® 7.5 mg, 22.5 mg-3 month, 30 mg-4 month,
45mg-6 month, and Lupron 2 week Kit

Diagnosis in Medicaid History of prostate cancer within last 2 years, AND

No Therapeutic Duplication with other strengths of Lupron.
Criterion 4 for Lupron-Depot 3.75 mg, 7.5 mg, 11.25 mg-3 month

Diagnosis in Medicaid History of breast cancer or ovarian cancer in the last 2
years, AND

No Therapeutic Duplication with other strengths of Lupron.
Additional criteria
Quantity limits apply
Lupron-Ped® criteria revision
 The point-of-sale approval requirement of the GnRH stimulation test for
CPP will be removed.
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria

Point-of-sale continuation criteria Lupron-Ped® injections: for those CPP
recipients previously approved who have 3 Lupron-Ped® paid claims in
the previous 6 months AND who are < age 11 years for females and < age
of 12 years for males. The continuation criteria were implemented on
Nov. 16, 2011.
Link to Memorandum
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Malathion (Ovide)
(Implemented 03/22/2006)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
Malathion Lotion
 > 6 years of age, AND
 History of at least one paid drug claim of permethrin or pyrethrin-piperonyl
in the last 28 days
Denial criteria



< 6 years of age, OR
History of one paid claim of malathion lotion in the last seven days, OR
History of two paid claims of malathion lotion in the last 28 days
Additional criteria
Quantity limits apply
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Macitentan (Opsumit) Tablet
(Implemented 03/18/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drug that requires a manual review for prior authorization

Opsumit 10 mg
Additional Criteria

Quantity Limits Apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Maraviroc (Selzentry)
(Implemented 04/12/2011)
Prescribers are required to fax a letter of medical necessity and include all
supporting documentation for manual review to 501-683-4124.
Drugs that require manual review for prior authorization

Selzentry
Link to Selzentry Form
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Mecamylamine HCL Tablet (Vecamyl)
(Implemented 09/18/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Vecamyl
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Meclorethamine HCL Gel (Valchlor)
(Implemented 03/18/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drug that requires a manual review for prior authorization

Valchlor 0.016% Gel
Additional Criteria

Quantity Limits Apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Medroxyprogesterone (Depo-Provera)
(Implemented 02/12/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval Criteria

No Therapeutic Duplication with any other injectable Depo-Provera
DESCRIPTION
MEDROXYPROGESTERONE ACETATE 104 MG/0.65 ML SYRINGE
MEDROXYPROGESTERONE ACETATE 150 MG/ML SYRINGE
MEDROXYPROGESTERONE ACETATE 150 MG/ML VIAL
MEDROXYPROGESTERONE ACETATE 400 MG/ML VIAL
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Megestrol (Megace and Megace ES)
(Implemented 10/18/2006)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria




History of HIV/AIDS in the past two years, OR
History of a paid claim for an antiviral: HIV agent in the past 60 days, OR
History of malignancy in the past two years, OR
History of a paid claim for an antineoplastic in the past 90 days
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Memantine XR (Namenda XR)
(Implemented 04/08/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria

>/= 90 days of Memantine XR therapy in the past 120 days
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Memantine Solution (Namenda)
(Implemented 09/18/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval Namenda:
 Age > 50 years of age, AND
 Diagnosis of NPO in the Medicaid History
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Meprobamate Tablet (Equanil)
(Implemented 07/09/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Mepron
(Implemented 09/21/2009)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that do not require prior authorization
Generic MAC’d sulfamethoxazole-trimethoprim tablets are available without a
prior authorization.
Drugs that require manual review for prior authorization

Mepron suspension
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Mercaptopurine 20mg/ml Suspension (Purixan)
(Implemented 01/13/2015)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual PA

Purixan
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Mesalamine 1000mg Suppository (Canasa)
(Implemented 06/21/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Methoxsalen Capsule (Oxsoralen-Ultra, 8-MOP)
(Implemented 09/23/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization


Oxsoralen-Ultra
8-MOP
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Metreleptin 11.3mg Vial (Myalept)
(Implemented 09/23/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Myalept Vial
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Metformin Oral Solution (Riomet)
(Implemented 09/21/2009)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria


Recipient </= 6 years of age, OR
Diagnosis of NPO in Medicaid history (Appendix A)
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Metformin Extended-Release (Fortamet ER, Glumetza
ER)
(Implemented 01/18/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that do not require prior authorization





Metformin 500 mg
Metformin 850 mg
Metformin 1000 mg
Metformin ER 500 mg
Metformin ER 750 mg
Drugs that require manual review for prior authorization


Fortamet ER
Glumetza ER
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Methotrexate Auto Inj. (Otrexup)
(Implemented 07/08/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual prior authorization

Otrexup
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Methotrexate Sodium (Trexall)
(Implemented 8/17/2010)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that do not require prior authorization

Methotrexate 2.5mg tablet
Drugs that require manual review for prior authorization




Trexall 5mg
Trexall 7.5mg
Trexall 10mg
Trexall 15mg
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Methscopolamine (Pamine, Pamine Forte, Pamine FQ)
(Implemented 06/19/2008)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria



History of peptic ulcer disease in Medicaid medical history in previous 6
months, AND
CPT code for H.Pylori in procedure history in the past 6 months, AND
At least 112 days of PPI therapy in the last 120 days.
Denial criteria
History of glaucoma
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Methylnaltrexone Br Sub-Q Injection (Relistor)
(Implemented 09/24/2008)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria



Medical diagnosis of malignant cancer in the past three years, AND
At least one paid Medicaid drug claim in the past 30 days for glycolax or
lactulose, AND
At least one paid Medicaid drug claim for an opioid in the past 30 days.
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Metoclopramide Orally Disentegrating Tablet (Metozolv
ODT)
(Implemented 01/12/2010)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that do not require prior authorization
Generic MAC’d metoclopropramide tablets and syrup are available without a
prior authorization.
Drugs that require manual review for prior authorization

Metozolv ODT tablet
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Metronidazole 375 mg capsule (Flagyl)
(Implemented 08/17/2010)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
o Diagnosis of NPO (Appendix A) in the previous 3 years, OR
o </= 6 years of age
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Metronidazole ER 750mg (Flagyl)
(Implemented 08/17/2010)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Flagyl 750 mg Tablets
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Metronidazole-Tetracycline-Bismuth (Helidac and
Pylera)
(Implemented 01/12/2005)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
Criterion 1:
 No history of lansoprazole, amoxicillin, and clarithromycin combination
(Prevpac) in the last 365 days, AND
 No history of omeprazole, amoxicillin, and clarithromycin combination
(Omeclamox-Pak) in the last 365 days, AND
Criterion 2:
 No history of metronidazole,tetracycline, and bismuth combination
(Helidac) in the last 365 days, OR
 No history of metronidazole, tetracycline, and bismuth combination
(Pylera) in the last 365 days.
Denial criteria
Criterion 1:
 History of lansoprazole, amoxicillin, and clarithromycin combination
(Prevpac) in the last 365 days, OR
 History of omeprazole, amoxicillin, and clarithromycin combination I
(Omeclamox-Pak) in the last 365 days,
Criterion 2:
 History of metronidazole, tetracyline, and bismuth combination (Helidac) in
the last 365 days, OR
 History of metronidazole, tetracyline, and bismuth combination (Pylera) in
the last 365 days
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Miconazole 50mg Buccal Tablet (Oravig)
(Implemented 01/18/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that do not require prior authorization


Clotrimazole 10mg troches
Nystatin 100,000 units/ml oral suspension
Drugs that require manual review for prior authorization

Oravig
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Miconazole Nitrate, Zinc Oxide, and White Petrolatum
Ointment (Vusion)
(Implemented 03/26/2008)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria

At least two paid claims for two different products from the following list in
the past 30 days:
 clotrimazole 1% cream,
 nystatin cream or ointment
 nystatin-trimacinolone cream or ointment
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Mifepristone 300mg Tablet (Korlym)
(Implemented 07/23/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Korlym
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Mig Lustat (Zavesca) Capsule
(Implemented 01/13/2015)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Zavesca
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Mipomersen Sodium Syringe (Kynamro)
(Implemented 07/09/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Kynamro
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Misoprostol (Cytotec)
(Implemented 01/09/2008)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
Criterion 1:
 Female, AND
 Long Term Care, OR
 Current birth control drug claim (within the past 30 days), OR
 Current injectable birth control drug claim, OR
 Medical history of tubal ligation, OR
 Medical history of hysterectomy, OR
 Medical history of menopause, OR
 Hormone replacement therapy in the past 45 days, OR
 Age > 55
AND
 NSAID claim in past 30 days
Criterion 2:
 Male, AND
 NSAID claim in the past 30 days
Denial criteria
Medical history of current pregnancy
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Modafinil (Provigil)
(Implemented 08/17/2005)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria


Age > 16 years of age, AND
History of at least one of the following in the last two years:
o Narcolepsy, OR
o Multiple sclerosis, OR
o Shift work sleep disorder, OR
o Obstructive sleep apnea/hypopnea, AND
 CPAP, OR
 BPAP, OR
 Nasal interface positive airway pressure device
Denial criteria


Age < 16 years of age, OR
History of at least one of the following in the last 30 days:
o Atomoxetine (Strattera), OR
o CII Stimulants, OR
o Other modafinil (Provigil) strengths, OR
o Other armodafinil (Nuvigil) strengths, OR
o Pemoline (Cylert)
Additional criteria
Quantity limits apply
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Mycophenolate (Cellcept, Myfortic)
(Suspension Implemented 10/11/2011)
(Capsules and Tablets Implemented 12/10/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria for Capsules and Tablets

Diagnosis of Organ Transplant in Medicaid History in the past 3 years
Approval criteria for Suspension



Diagnosis of Organ Transplant in Medicaid History in the past 3 years
< 6 years of age, OR
NPO (Appendix A)
Link to Memorandum
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Nabilone (Cesamet)
(Implemented 06/27/2007)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria





Age > 18 years of age, AND
Submitted ICD-9 diagnosis malignant cancer within the past 365 days,
AND
o Paid drug claim in history for antineoplastic agents within the past 45
days, OR
o Procedure code indicating radiation treatment within the past 45
days,
AND
Paid drug claim in history within the past 45 days for an oral 5-HT3
(serotonin) receptor antagonist, OR
Paid drug claim in history within the past 45 days for a NK1 (neurokinin-1)
receptor antagonist, OR
Paid drug claim in history within the past 45 days for Marinol.
Denial criteria





Absence of approval criteria
Submitted ICD-9 diagnosis bipolar in medical history.
Submitted ICD-9 diagnosis depression in medical history.
Submitted ICD-9 diagnosis schizophrenia in medical history.
Submitted ICD-9 diagnosis substance or alcohol abuse in medical history.
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Nafarelin Nasal Spray (Synarel)
(Implemented 09/21/2009)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria


Diagnosis of central precocious puberty (CPP) in the previous three years,
OR
Diagnosis of endometriosis in the previous three years
Denial criteria
Diagnosis of infertility in the previous three years
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Naloxone Auto-Injector (Evzio)
(Implemented 09/23/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Evzio 0.4mg Auto-Injector
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Nandrolone Decanoate Injection
(Implemented 01/09/2008)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria



Diagnosis for anemia secondary to chronic renal failure in the past 90
days, AND
At least three paid Medicaid claims in the past 90 days for erythropoietin,
AND
No therapeutic duplication with erythropoietin
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Neuropathic Pain Agents
(Implemented 06/05/2008)
The non-preferred antiepileptic medications will be considered non-preferred for
treating fibromyalgia and neuropathic pain only. Medications listed as either
preferred or non-preferred status in this category may or may not include an FDA
approved indication for fibromyalgia or neuropathic pain. Use of these
medications for fibromyalgia, neuralgias, and neuropathic pain has been
reviewed through the evidence-based review process. Medications listed in this
category as either preferred or nonpreferred status are not to be construed as
endorsements for marketing of off-label use by the manufacturer or by Medicaid.
Prescribers may request an override for nonpreferred drugs by calling the
UAMS College of Pharmacy Evidence-Based Prescription Drug Program
Help Desk at 1-866-250-2518 (toll-free) or 501-526-4200 (local).
Preferred agents





Amitriptyline HCl (Elavil)
Carbamazepine chewable tablet (Tegretol Chewable)
Carbamazepine immediate-release tablet (Tegretol)
Gabapentin 100mg, 300mg, 400mg capsule (Neurontin)
Nortriptyline HCl (Pamelor)
Preferred agents with criteria

Venlafaxine HCl (Effexor) – see Second Generation Antidepressant
Nonpreferred agents:


Gabapentin extended-release capsule (Gralise ER)
Gabapentin enacarbil extended-release tablet (Horizant ER)
Nonpreferred agents with criteria:













Carbamazepine extended-release capsule (Carbatrol SA, Equetro)
Carbamazepine extended-release tablet (Tegretol XR)
Carbamazepine Suspension (Tegretol)
Divalproex sodium (Depakote)
Duloxetine HCl (Cymbalta) – see Second Generation Antidepressant
Gabapentin 250mg/5ml solution (Neurontin)
Gabapentin 100mg, 200mg, 400mg, 600mg, 800mg tablet (Neurontin)
Lacosamide (Vimpat)
Lamotrigine (Lamictal)
Lidocaine patch (Lidoderm)
Oxcarbazepine (Trileptal)
Pregabalin (Lyrica)
Topiramate (Topamax)
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria


Valprioc acid (Depakene, Stavzor)
Venlafaxine HCl extended-release capsule (Effexor XR) – see Second
Generation Antidepressant
Approval criteria for pregabalin (Lyrica)
 One or more of the approved diagnosis (Appendix H), AND
 No therapeutic duplication with pregabalin, OR
 One therapeutic duplication (75% overlap of last fill) with different date of
service and same prescriber ID between Lyrica GCNs in previous 93 days,
AND
 No diagnosis of myalgia and myositis, unspecified (ICD-9 729.1) in the past
three years
Approval criteria for nonpreferred anti-epileptic agents
Nonpreferred Antiepileptic Agents:
Antiepileptic
Carbamazepine extended-release capsule (Carbatrol ER, Equetro)
Carbamazepine extended-release tablet (Tegretol XR)
Carbamazepine suspension (Tegretol)
Divalproex sodium (Depakote)
Gabapentin 250mg/5ml solution (Neurontin)
Gabapentin 600mg, and 800mg tablet (Neurontin)
Lamotrigine (Lamictal)
Oxcarbazepine (Trileptal)
Pregabalin (Lyrica)
Topiramate (Topamax)
Valprioc acid (Depakene, Stavzor)


One or more of the approved diagnoses (Appendix H)
No diagnosis of myalgia and myositis, unspecified (ICD-9 729.1) in the past
three years – see Fibromyalgia agent criteria
Nonpreferred lamotrigine ODT (Lamictal ODT) and topiramate sprinkle
capsules (Topamax Sprinkles)
 One or more of the approved diagnoses (Appendix H), AND
 Age ≤ 6, OR
 NPO (Appendix A)
Nonpreferred extended-release products (Carbatrol ER, Depakote ER,
Equetro,Gralise ER, Horizant ER, Lamictal XR, Oxtellar XR, Stavzor XR,
Tegretol XR)
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria

>/= 90 days of therapy of the same extended-release product in the past 120
days. Immediate-release products are covered via existing criteria
Approval criteria for nonpreferred topical analgesia


Submitted ICD-9 diagnosis post-herpetic neuralgia (Table 4) within the past
12 months, OR
Paid claim in history identifying appropriate antiviral medication (Table 4.2)
for post-herpetic neuralgia (Table 4) within the past 30 days
Table 4 – Postherpetic neuralgia diagnoses
ICD-9
53.12
53.13
Description
Postherpetic trigeminal neuralgia
Postherpetic polyneuropathy
Table 4.2 – Anitvirals
Antivirals
Acyclovir 200mg
Acyclovir 200mg
Acyclovir 400mg
Acyclovir 800mg
Famciclovir 125mg
Famciclovir 250mg
Famciclovir 500mg
Valacyclovir 1g caplet
Valacyclovir 500mg caplet
Link to Memorandum
Link to Memorandum Lamictal ODT
Link to Memorandum Lidoderm Patch
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Nevirapine XR (Viramune XR)
(Implemented 04/08/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria

>/= 90 days of Nevirapine XR therapy in the past 120 days
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Nevirapine Oral Supension (Viramune)
(Implemented 09/18/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval Razadyne:
 Age </= 6 Years of Age
 Diagnosis of NPO in the Medicaid History
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Nimodipine Solution (Nymalize)
(Implemented 1210/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Nymalize Solution
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Nitisinone Capsule (Orfadin)
(Implemented 09/23/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Orfadin Capsule
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Nitrofurantoin Suspension (Furadantin)
(Implemented 10/11/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria


< 6 years of age, OR
NPO (Appendix A)
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Nitroglycerin 0.4% Rectal Ointment (Rectiv)
(Implemented 07/09/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization
Rective Rectal Ointment
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Non-benzodiazepine Sedative Hypnotics
(Implemented 03/01/2009)
Prescribers may request an override for nonpreferred drugs by calling the
UAMS College of Pharmacy Evidence-Based Prescription Drug Program
Help Desk at 1-866-250-2518 (toll-free) or 501-526-4200 (local).
Preferred agents with criteria


Zaleplon (Sonata)
Zolpidem immediate-release (Ambien)
Nonpreferred agents






Eszopiclone (Lunesta)
Doxepine (Silenor)
Ramelton (Rozerem)
Suvorexant (Belsomra)
Zolpidem extended-release (Ambien CR)
Zolpidem sublingual tablet (Edluar, Intermezzo)
Approval criteria for preferred agents with criteria
No therapeutic duplication with other sedative hypnotics
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Nizatadine Oral Solution (Axid)
(Implemented 12/10/2008)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria



At least two paid Medicaid drug claims for ranitidine syrup in the past 60
days, AND
< 6 years of age, OR
NPO (Appendix A)
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Noxafil DR Oral Tablet and Noxafil 300mg Vial
(Implemented 07/08/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Noxafil DR Oral Tablet

Noxafil 300mg Vial
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Omega-3-acid ethyl esters (Lovaza)
(Implemented 09/18/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Lovaza
Additional Criteria

Quantity Limits Apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Omeprazole, Amoxicillin, and Clarithromycin
combination (Omeclamox-Pak)
(Implemented 05/21/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
Criterion 1:
 No history of lansoprazole, amoxicillin, and clarithromycin combination
(Prevpac) in the last 365 days, AND,
 No history of omeprazole, amoxicillin, and clarithromycin combination
(Omeclamox-Pak) in the last 365 days, AND,
 No concurrent proton pump inhibitor therapy within the past 30 days.
Criterion 2:
 No history of lansoprazole, amoxicillin, and clarithromycin combination
(Prevpac) in the last 365 days, AND,
 No history of omeprazole, amoxicillin, and clarithromycin combination
(Omeclamox-Pak) in the last 365 days, AND,
 No concurrent proton pump inhibitor therapy within the past 30 days.
Criterion 3:
 No history of metronidazole/tetracycline/bismuth combination (Helidac) in
the last 365 days, OR
 No history of metronidazole/tetracycline/bismuth combination (Pylera) in
the last 365 days.
Denial criteria
Criterion 1:
 History of lansoprazole, amoxicillin, and clarithromycin combination
(Prevpac) in the last 365 days, OR
 Current proton pump inhibitor therapy within the past 30 days
Criterion 2:
 No history of omeprazole, amoxicillin, and clarithromycin combination
(Omeclamox-Pak) in the last 365 days, AND,
 No concurrent proton pump inhibitor therapy within the past 30 days.
Criterion 3:
 No history of metronidazole/tetracycline/bismuth combination (Helidac) in
the last 365 days, OR
 No history of metronidazole/tetracycline/bismuth combination (Pylera) in
the last 365 days.
Additional criteria
Quantity limits apply
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Opioids, Long-acting
(Implemented 08/01/2008)
Prescribers may request an override for nonpreferred drugs by calling the
UAMS College of Pharmacy Evidence-Based Prescription Drug Program
Help Desk at 1-866-250-2518 (toll-free) or 501-526-4200 (local).
Preferred agents with criteria


Methadone HCl (Dolophine)
Morphine sulfate long-acting tablet (MS Contin, Oramorph)
Nonpreferred agents with criteria









Buprenorphine patch (Butrans)
Fentanyl patch (Duragesic)
Hydromorphone HCl extended-release tablet (Exalgo ER)
Morphine sulfate extended-release capsule (Avinza, Kadian)
Morphine sulfate/naltrexone (Embeda)
Oxycodone-Acetaminophen extended-release tablet (Xartemis XR)
Oxycodone extended-release tablet (Oxycontin)
Oxymorphone HCl extended-release tablet (Opana ER)
Tapentadol HCl extended-release tablet (Nucynta ER)
Approval criteria for preferred agents with criteria

No therapeutic duplication in drug history between long-acting narcotics
Approval criteria for nonpreferred agents with criteria


Buprenorphine patch
o NPO (Appendix A), OR
o Currently LTC, OR
o Cancer with malignancies (Appendix E) or antineoplastic drug
history (Appendix F) in past 12 months
AND
o No therapeutic duplication in drug history between long-acting
narcotics
Fentanyl patch
o NPO (Appendix A), OR
o Currently LTC, OR
o Cancer with malignancies (Appendix E) or antineoplastic drug
history (Appendix F) in past 12 months
AND
o No therapeutic duplication in drug history between long-acting
narcotics
 Morphine sulfate long-acting capsule or oxycodone long acting tablet
o Currently LTC, OR
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Cancer with malignancies (Appendix E) or antineoplastic drug
history (Appendix F) in past 12 months
AND
o No therapeutic duplication in drug history between long-acting
narcotics
o
Denial criteria
Paid claim for Suboxone or Subutex in the past 60 days
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Opioids, Short-acting
(Implemented 11/12/2008)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria







Accumulation quantity limit will allow up to a maximum of 124 units of any
solid oral short acting opioid paid by Medicaid per the previous 31
calendar days.
No drug claim in the past 60 days for Subutex, OR
No drug claim in the past 60 days for Suboxone
AND
Therapeutic duplication between short-acting opioids with less than 25%
of the days’ supply remaining on the previous claim, OR
Therapeutic duplication between a short-acting opioid and tramadol IR
(Ultram) with less than 25% of the days’ supply remaining on the previous
claim, OR
Therapeutic duplication between a short-acting opioid and
tramadol/acetaminophen (Ultracet) with less than 25% of the days’ supply
remaining on the previous claim
Therapeutic duplication between a short-acting opioid and tramadol ODT
(Rybix) with less than 25% of the days’ supply remaining on the previous
claim
Denial criteria







Therapeutic duplication between two short-acting opioids with more than
25% of the days’ supply remaining on previous claim
Therapeutic duplication between a short-acting opioid and tramadol
(Utram and Ultracet) with more than 25% of the days’ supply remaining on
previous claim
Therapeutic duplication between a short-acting opioid and tramadol ODT
(Rybix) with more than 25% of the days’ supply remaining on previous
claim
Drug claim in history for Subutex
Drug claim in history for Suboxone
Solid oral dosage forms for short-acting opioids will reject for children less
than 6 years of age.
Greater than 124 units of any solid oral short acting opioid paid by
Medicaid per the previous 31 calendar days.
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Exemptions

Patients who have a diagnosis of malignant cancer or a paid claim for an
antineoplastic in the past 12 months are exempt from the therapeutic
duplication requirement. Quantity restrictions still apply.
Short-acting pain medications that process with point of sale prior
authorization criteria
POINT OF SALE APPROVED SHORT-ACTING PAIN MEDICATIONS
ACETAMINOPHEN-CODEINE 300-15 MG TABLET
COMMON or OLDER TRADE NAME
ACETAMINOPHEN-CODEINE 120-12 MG/5 ML
SOLUTION
TYLENOL WITH CODEINE #2
ACETAMINOPHEN-CODEINE 300-30 MG TABLET
TYLENOL WITH CODEINE #3
ACETAMINOPHEN-CODEINE 300-60 MG TABLET
BUTALBITAL-ACETAMINOPHEN-CAFFEINE 50-325 MG/15 ML
SOLUTION
BUTALBITAL-ACETAMINOPHEN 50-325 MG TABLET
BUTALBITAL-ACETAMINOPHEN-CAFFEINE 50-325-40 MG
TABLET
CODEINE SULFATE 15 MG TABLET
TYLENOL WITH CODEINE #4
ACETAMINOPHEN-CODEINE 120-12 MG/5 ML SOLUTION
ALAGESIC LQ SOLUTION
PHRENILIN TABLET
ESGIC TABLET
CODEINE SULFATE 30 MG TABLET
CODEINE SULFATE 15 MG TABLET
CODEINE SULFATE 30 MG/5 ML ORAL
SOLUTION
CODEINE SULFATE 30 MG TABLET
CODEINE SULFATE 60 MG TABLET
CODEINE SULFATE 60 MG TABLET
HYDROCODONE-ACETAMINOPHEN 5-325 MG TABLET
NORCO 5-325 TABLET
HYDROCODONE-ACETAMINOPHEN 7.5-325 MG TABLET
NORCO 7.5-325 TABLET
HYDROCODONE-ACETAMINOPHEN 7.5-325 MG/15 ML SOLUTION
HYCET 7.5-325 MG/5 ML SOLUTION
HYDROCODONE-ACETAMINOPHEN 10-300 MG/15 ML SOLUTION
LORTAB 10-300 MG/15 ML SOLUTION
HYDROCODONE-ACETAMINOPHEN 10-325 MG TABLET
NORCO 10-325 TABLET
HYDROCODONE-IBUPROFEN 5-200 MG TABLET
IBUDONE 5-200 MG TABLET
HYDROCODONE-IBUPROFEN 5-200 MG TABLET
REPREXAIN 5-200 MG TABLET
HYDROCODONE-IBUPROFEN 7.5-200 MG TABLET
VICOPROFEN 7.5-200 TABLET
HYDROCODONE-IBUPROFEN 10-200 MG TABLET
IBUDONE 10-200 MG TABLET
HYDROCODONE-IBUPROFEN 10-200 MG TABLET
REPREXAIN 10-200 MG TABLET
HYDROMORPHONE 1 MG/ML LIQUID
DILAUDID LIQUID
HYDROMORPHONE 2 MG TABLET
DILAUDID 2 MG TABLET
HYDROMORPHONE 4 MG TABLET
DILAUDID 4 MG TABLET
HYDROMORPHONE 8 MG TABLET
DILAUDID 8 MG TABLET
CODEINE SULFATE 30 MG/5 ML SOLUTION
LEVORPHANOL TARTRATE 2 MG TABLET
LEVO-DROMORAN 2 MG TAB
MEPERIDINE 50 MG TABLET
DEMEROL 50 MG TABLET
MEPERIDINE 100 MG TABLET
DEMEROL 100 MG TABLET
MORPHINE SULFATE 10 MG/5 ML SOLUTION
MSIR 10 MG/5 ML ORAL SOLUTION
MORPHINE SULFATE 15 MG TABLET
MSIR 15 MG TABLET
MORPHINE SULFATE 20 MG/ML CONCENTRATED SOLUTION
ROXANOL 20 MG/ML CONCENTRATE
MORPHINE SULFATE 20 MG/5 ML SOLUTION
MSIR 20 MG/5 ML ORAL SOLUTION
MORPHINE SULFATE 30 MG TABLET
MSIR 30 MG TABLET
OXYCODONE 5 MG CAPSULE
OXYIR 5 MG CAPSULE
OXYCODONE 5 MG/5 ML SOLUTION
OXYCODONE 5 MG/5 ML SOLUTION
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
POINT OF SALE APPROVED SHORT-ACTING PAIN MEDICATIONS
OXYCODONE 5 MG TABLET
COMMON or OLDER TRADE NAME
ROXICODONE 5 MG TABLET
OXYCODONE 10 MG TABLET
OXYCODONE 10 MG TABLET
OXYCODONE 15 MG TABLET
ROXICODONE 15 MG TABLET
OXYCODONE 20 MG TABLET
OXYCODONE 20 MG TABLET
OXYCODONE 30 MG TABLET
OXYCODONE 30 MG TABLET
OXYCODONE-ACETAMINOPHEN 5-325 MG/5 ML SOLUTION
ROXICET 5-325 MG/5 ML SOLUTION
OXYCODONE -ACETAMINOPHEN 5-325 MG TABLET
PERCOCET 5-325 TABLET
OXYCODONE-ACETAMINOPHEN 7.5-325 MG TABLET
PERCOCET 7.5-325 TABLET
OXYCODONE-ACETAMINOPHEN 10-325 MG TABLET
PERCOCET 10-325 TABLET
TRAMADOL 50 MG TABLET
ULTRAM TABLET
TRAMADOL-ACETAMINOPHEN 37.5-325 MG TABLET
ULTRACET TABLET
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Short-Acting pain medications that require manual review for prior
authorization
MANUALLY REVIEWED SHORT-ACTING PAIN MEDICATIONS
ACETAMINOPHEN-CODEINE 120-12 MG/5 ML SUSPENSION
COMMON TRADE NAME
CAPITAL WITH CODEINE SUSPENSION
BUTALBITAL-ACETAMINOPHEN 50-300 MG TABLET
BUPAP 50-300 MG TABLET
BUTALBITAL-ACETAMINOPHEN-CAFFEINE 50-300-40 MG CAPSULE
FIORICET CAPSULE
BUTALBITAL-ACETAMINOPHEN-CAFFEINE 50-325-40 MG CAPSULE
ESGIC CAPSULE
BUTALBITAL-ASPIRIN-CAFFEINE 50-325-40 MG CAPSULE
FIORINAL CAPSULE
BUTORPHANOL 10 MG/ML NASAL SPRAY
CODEINE-BUTALBITAL-ACETAMINOPHEN-CAFFEINE 30-50-325-40
MG CAPSULE
CODEINE-BUTALBITAL-ASPIRIN-CAFFEINE 30-50-325-40 MG
CAPSULE
DIHYDROCODEINE-ASPIRIN-CAFFEINE 16-356-30 MG CAPSULE
STADOL NASAL SPRAY
HYDROCODONE-ACETAMINOPHEN 2.5-325 MG TABLET
VERDROCET 2.5-325 MG TABLET
HYDROCODONE-ACETAMINOPHEN 5-300 MG TABLET
VICODIN 5-300 MG TABLET
HYDROCODONE-ACETAMINOPHEN 7.5-300 MG TABLET
VICODIN ES 7.5-300 MG TABLET
HYDROCODONE-ACETAMINOPHEN 10-300 MG TABLET
VICODIN HP 10-300 MG TABLET
HYDROCODONE-ACETAMINOPHEN 10-325 MG/15 ML SOLUTION
ZAMICET 10-325 MG/15 ML SOLUTION
HYDROCODONE-IBUPROFEN 2.5-200 MG TABLET
REPREXAIN 2.5-200 MG TABLET
OPIUM TINCTURE 10 MG/ML LIQUID
OXYCODONE-ACETAMINOPHEN 2.5-325 MG TABLET
OPIUM TINCTURE 10 MG/ML ORAL LIQUID
OXYCODONE 20 MG/ML CONCENTRATED
ORAL SOLN
PERCOCET 2.5-325 MG TABLET
OXYCODONE-ACETAMINOPHEN 5-300 MG TABLET
PRIMLEV 5-300 MG TABLET
OXYCODONE-ACETAMINOPHEN 5-400 MG TABLET
MAGNACET 5-400 MG TABLET
OXYCODONE-ACETAMINOPHEN 7.5-300 MG TABLET
PRIMLEV 7.5-300 MG TABLET
OXYMORPHONE 5 MG TABLET
OPANA 5 MG TABLET
OXYMORPHONE 10 MG TABLET
OPANA 10 MG TABLET
PENTAZOCINE-NALOXONE 50-0.5 MG TABLET
TALWIN NX TABLET
TAPENTADOL 50 MG TABLET
NUCYNTA 50 MG TABLET
TAPENTADOL 75 MG TABLET
NUCYNTA 75 MG TABLET
TAPENTADOL 100 MG TABLET
NUCYNTA 100 MG TABLET
OXYCODONE 20 MG/ML CONCENTRATED SOLUTION
Additional criteria
Quantity limits apply
Link to Memorandum
Link to Memorandum
FIORICET WITH CODEINE CAPSULE
FIORINAL WITH CODEINE CAPSULE
SYNALGOS-DC CAPSULE
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Link to Memorandum
Link to updated criteria
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Opium Tincture
(Implemented 10/11/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Opium Tincture
Additional Criteria

Quantity Limits Apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Oseltamivir Suspension (Tamiflu)
(Implemented 10/11/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria


≤ 12 years of age, AND
At least 1 year of age
Additional criteria

Quantity Limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Osteoporosis drugs
(Implemented 08/17/2010)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that do not require prior authorization





Alendronate sodium 5mg daily dose (Fosamax®)
Alendronate sodium 10mg daily dose (Fosamax®)
Alendronate sodium 35mg weekly dose (Fosamax®)
Alendronate sodium 40mg weekly dose (Fosamax®)
Alendronate sodium 70mg weekly dose (Fosamax®)
Drugs that require manual review for prior authorization








Actonel® tablet
Binosto® effervescent tablet
Boniva ® tablet
Boniva® injection
Fosamax® Plus D tablet
Fosamax® oral solution
Forteo® injection (new start only)
Prolia® injection (see below):
Prolia
Prolia® will continue to be covered through a manual review PA on a case-bycase basis for the initial dose. POS PA continuation approval criteria for Prolia®
will apply as follows:
 1 Prolia® claim is found in Medicaid drug history in the previous 12
months.
 In addition, a therapeutic duplication edit will reject an incoming Prolia®
claim if an Xgeva® (denosumab) claim is found in the medical claims
history in previous 6 months.
 A quantity edit for Prolia® of 1 injection per 175 days will be implemented.
Additional criteria

Forteo® quantity limits apply
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Link to Memorandum
Link to Memorandum (Prolia)
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Otic Preparations
(Implemented 09/21/2009, 01/18/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
OTIC PREPARATIONS
GENERIC NAME
COMMON TRADE NAME*
PA STATUS
Acetic Acid 2% otic drops
Acetic Acid 2% otic solution
No PA
Antipyrine-Benzocaine-Glycerin otic solution
Aurodex® otic solution
No PA
Benzocaine 20% otic drops
Pinnacaine® 20% otic drops
No PA
Ciprofloxacin 0.3% ophthalmic drops
Ciloxan® 0.3% ophthalmic drops
No PA
Fluocinolone acetonide Oil otic drops
Dermotic® Oil 0.01% otic drops
No PA
Neomycin sulfate-Polymyxin B-Hydrocortisone otic
solution or suspension
Cortisporin® Ear otic solution or
suspension
No PA
Ofloxacin 0.3% otic drops
Floxin® 0.3% otic drops
No PA
Sulfacetamide-Prednisolone 10-0.23% ophthalmic
drops
Sulf-Pred® 10-0.23% ophthalmic
drops
No PA
GENERIC NAME
COMMON TRADE NAME*
PA STATUS
Acetic Acid-Hydrocortisone otic drops
Acetasol HC® otic drops
Manual PA
Acetic Acid-Benzocaine 5.5%-1.4% otic drops
Aurax® otic solution
Manual PA
Antipyrine-Benzocaine-Zinc Acetate otic drops
Otozin® otic solution
Manual PA
Ciprofloxacin-Dexamethasone otic suspension
Ciprodex® otic suspension
Manual PA
Ciprofloxacin-Hydrocortisone otic suspension
Cipro HC® otic suspension
Manual PA
Neomycin sulfate-Polymyxin B-HydrocortisoneThonzonium otic drops
Coly-Mycin S® otic drops
Manual PA
Neomycin sulfate-Polymyxin B-HydrocortisoneThonzonium otic drops
Cortisporin TC® otic suspension
Manual PA
Link to Memorandum Otic Preparations Implemented 01/18/2011
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Overactive-bladder Agents
(Implemented 07/14/2009)
Prescribers may request an override for nonpreferred drugs by calling the
UAMS College of Pharmacy Evidence-Based Prescription Drug Program
Help Desk at 1-866-250-2518 (toll-free) or 501-526-4200 (local).
Preferred agents



Fesoterodine fumarate (Toviaz)
Oxybutynin chloride 5mg/5ml Syrup, 5mg tablet (Ditropan)
Solfenacin succinate (Vesicare)
Preferred agents with criteria

Oxybutynin chloride extended-release tablet (Ditropan XL Tablet)
Nonpreferred agents









Darifenacin hydrobromide (Enablex)
Flavoxate HCl (Urispas)
Mirabegron extended-release (Myrbetriq)
Oxybutynin chloride gel (Gelnique)
Oxybutynin patch (Oxytrol)
Tolterodine tartrate tablet (Detrol)
Tolterodine tartrate extended-release capsule (Detrol LA)
Trospium chloride extended-release (Sanctura XR)
Trospium chloride immediate-release (Sanctura)
Approval criteria for preferred agents with criteria

Oxybutynin XL tablet
 Ages 6 – 18, AND
 Diagnosis of spina bifida (ICD-9: 741), OR
 Four paid claims of oxybutynin XL in the past 6 months and age
between 6 – 18
Link to PDL Memorandum: Overactive-bladder agents
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Oxandrolone (Oxandrin)
(Implemented 01/09/2008)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
Criterion 1:
Diagnosis in the past two years for:
 HIV/AIDS, AND
 Cachexia
AND
 Paid drug claims in history for at least three antiretrovirals (either as a
single entity or combo drug) within the past 30 days, AND
 Paid drug claim in history for megestrol acetate within the last four weeks
Criterion 2:
Diagnosis code in Medicaid history in the past 365 days for one of the following:
 Weight loss secondary to severe trauma (burns, spinal cord injury), OR
 Weight loss due to protein catabolism associated with prolonged
administration of high dose corticosteroids.
Criterion 3:
 Diagnosis in Medicaid history for osteoporosis, AND
 Concurrent therapy in the past 45 days for one of the following:
o Biphophonate
 Didronel (etidronate)
 Fosamax (alendronate)
o Aminobisphosphonate
 Actonel (risedronate)
o Selective estrogen-receptor modulators
 Evista (raloxifene)
 Calcitonin injection, OR
 History of Ibandronate in the past 100 days
Criterion 4:
 Diagnosis in Medicaid history for hereditary angioedema in the past three
years.
Denial criteria
Diagnosis in Medicaid history for any of the following in the past 365 days:
 Prostate cancer
 Breast cancer – male or female
 Pregnancy
 Nephrosis
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Oxymethalone (Anadrol—50 tablet)
(Implemented 01/09/2008)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
Criterion 1:
 Diagnosis of acquired aplastic anemia in the past 365 days, AND
 Five claims in the past six months for Cyclosporine
Criterion 2:
 Diagnosis of chronic renal failure in the past 365 days, AND
 History of three paid drug claims of recombinant erythropoietin in the past
90 days
Criterion 3:
 Diagnosis of malignant cancer in the past 365 days, AND
 Paid drug claim for an antineoplastic in the past 365 days, AND
 History of three paid drug claims for Neupogen in the past 90 days, OR
 History of three paid drug claims for Neulasta in the past 90 days
Criterion 4:
 Diagnosis of Fanconi’s anemia in the past 365 days
Criterion 5:
 Diagnosis for congenital refractory pure red cell aplasia in the past 365
days,
AND
 At least 30 days of corticosteroid therapy in the past 90 days
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Pain Medications, Injectable
(Implemented 04/12/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Injectable agents








Buprenorphine Injectable
Butorphanol Injectable
Hydromorphone Injectable
Levorphanol Injectable
Meperidine Injectable
Morphine Injectable
Nalbuphine Injectable
Pentazocine Injectable
Approval criteria






No drug claim in the past 60 days for Subutex, OR
No drug claim in the past 60 days for Suboxone
AND
Therapeutic duplication between short-acting opioids with less than 25%
of the days’ supply remaining on the previous claim, OR
Therapeutic duplication between a short-acting opioid and tramadol IR
(Ultram) with less than 25% of the days’ supply remaining on the previous
claim, OR
Therapeutic duplication between a short-acting opioid and
tramadol/acetaminophen (Ultracet) with less than 25% of the days’ supply
remaining on the previous claim
Therapeutic duplication between a short-acting opioid and tramadol ODT
(Rybix) with less than 25% of the days’ supply remaining on the previous
claim
Denial criteria





Therapeutic duplication between two short-acting opioids with more than
25% of the days’ supply remaining on previous claim
Therapeutic duplication between a short-acting opioid and tramadol
(Utram and Ultracet) with more than 25% of the days’ supply remaining on
previous claim
Therapeutic duplication between a short-acting opioid and tramadol ODT
(Rybix) with more than 25% of the days’ supply remaining on previous
claim
Drug claim in history for Subutex
Drug claim in history for Suboxone
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Exemptions
Patients who have a diagnosis of malignant cancer or a paid claim for an
antineoplastic in the past 12 months are exempt.
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Papaverine 30mg/ml
(Implemented 08/10/2007)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Denial criteria


Submitted ICD-9 diagnosis for erectile dysfunction
Submitted ICD-9 diagnosis for Impotence
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Pasireotide Diaspartate (Signifor) Ampule
(Implemented 09/18/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Signifor
Additional Criteria

Quantity Limits Apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Pazopanib (Votrient)
(Implemented 10/10/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Votrient
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
PegInterferon Alfa-2B (Sylatron)
(Implemented 05/25/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Denial criteria

Submitted ICD-9 diagnosis for Hepatitis C, Chronic and Acute
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Pegvisomant Injection (Somavert)
(Implemented 04/17/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
No Therapeutic duplication allowed between different strengths of Somavert
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Penicillamine (Depen 250mg; Cuprimine 250mg)
(Implemented 09/18/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization


Depen 250mg Tablet
Cuprimine 250mg Capsule
Additional Criteria

Quantity Limits Apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Perampanel Tablet (Fycompa)
(Implemented 07/08/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Fycompa
Additional Criteria

Quantity Limits Apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Phosphate Removing Agents
(Implemented 07/08/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that do not require prior authorization





Calcium acetate 667 mg Capsule [PhosLo]
Calcium acetate 667 mg/5 ml Solution [Phoslyra]
Calcium acetate 667 mg Tablet [Eliphos]
Sevelamer HCl Tablet [Renagel]
Sevelamer carbonate 800 mg Tablet [Renvela 800 mg Tablet]
Drugs that require manual review for prior authorization




Ferric Citrate Tablet
Lanthanum carbonate Chewable Tablet [Fosrenol]
Sevelamer carbonate Powder Packet [Renvela Powder Packet]
Sucroferric oxyhydroxide Chewable Tablets [Velphoro]
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Pimecrolimus (Elidel)
(Implemented 03/12/2007)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria



No therapeutic duplication with Tacrolimus (Protopic), AND
At least two paid Medicaid drug claims of topical corticosteroid agents,
each containing a different drug entity, AND
At least one of the claims for the topical corticosteroid being at least
medium potency or higher filled in the previous 14-45 day period.
Additional criteria


Age > 2 years of age
Quantity limits apply
Denial criteria




History of Psoriasis in previous two years
Therapeutic duplication with Tacrolimus (Protopic)
No claim for at least two topical corticosteroids in Medicaid history
No claim for a medium potency or higher topical corticosteroid in the
previous 14-45 day period.
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Podofilox (Condylox 0.5% topical solution and gel)
(Implemented 01/09/2008)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
Podofilox 0.5% Topical Solution (Condylox)
 ≥ 18 years of age, AND
 No therapeutic duplication with Podofilox 0.5% gel, AND
 Diagnosis of Condyloma Acuminanta (commonly known as external
genital or perianal warts) within the past two months
Podofilox 0.5% Topical Gel (Condylox)
 ≥ 18 years of age, AND
 No therapeutic duplication with Podofilox 0.5% solution, AND
 Diagnosis of of Condyloma Acuminanta (commonly known as external
genital or perianal warts) within the past two months OR
Denial criteria



Absence of approval criteria
< 18 years of age
Therapeutic duplication of gel/solution
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Pomalidomide Capsule (Pomalyst)
(Implemented 07/09/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Pomalyst
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Ponatinib HCl Tablet (Iclusig)
(Implemented 07/09/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Iclusig
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Posaconazole (Noxafil) Suspension
(Implemented 01/09/2008)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
Criterion 1:
Diagnosis code in Medicaid history for at least one of the following in the past
365 days:
 ≥ 13 years of age, AND
 HIV/AIDS
 Organ transplant procedure
 Graft vs. host disease
 Neutropenia
Criterion 2:
The following drug claims in Medicaid history in the past 365 days:
 ≥ 13 years of age, AND
 HIV/AIDS pharmacotherapy drug claims in history, OR
 Anti-rejection/Immunosuppression medication
Criterion 3:
 ≥ 13 years of age, AND
 At least one paid claim for Fluconazole in the past 30 days, AND
 At least one paid claim for Itraconazole in the past 30days.
Criterion 4:
 ≥ 13 years of age, AND
 History of paid claim for requested drug (Noxafil) in the past 180 days.
Denial criteria



< 13 years of age
Absence of approval criteria
History of a paid drug claim for the any of the following in the last 30 days:
o Ergot alkaloids
o Pimozide
o Quinidine
Link to Memorandum
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Posaconazole (Noxafil DR 100mg Oral Tablet and
Noxafil 300mg Vial)
(Implemented 07/08/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization


Noxafil DR 100mg Tablet
Noxafil 300mg Vial
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Potassium Chloride (KCl) Capsule and Packet
(Implemented 10/10/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that do not require prior authorization





Potassium chloride 8 mEq extended release-tablet [Klor-Con 8 mEq
tablet]
Potassium chloride 10 mEq extended-release tablet [Klor-Con M10]
Potassium chloride 10% (20 mEq/15 ml) oral solution
Potassium chloride 20 mEq extended-release tablet [Klor-Con M20]
Potassium chloride 25 mEq effervescent tablet [Effer-K, Klor-Con-EF]
Drugs that require manual review for prior authorization




Potassium chloride 8 mEq extended-release capsule [Micro-K]
Potassium chloride 10 mEq extended-release capsule [Micro-K]
Potassium chloride 20 mEq powder packet [Klor-Con 20 mEq packet]*
Potassium chloride 25 mEq powder packet [Klor-Con 25 mEq packet)
*Effective 4/14/2014
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Pramipexole ER (Mirapex ER)
(Implemented 03/19/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria


Diagnosis of Parkinson’s Disease in Medicaid history in previous 2 years,
AND
>/= 90 days of therapy of Pramipexole ER in the past 120 days
Link to Memorandum
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Prednisolone
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that do not require prior authorization





Generic prednisolone sodium phosphate 15mg/5ml (same as Orapred ®
Solution) is available without a prior authorization
Methylprednisolone Dose Pack
Methylprednisolone tablet
Prednisone Dose Pack
Prednisone tablet
Drugs that require manual review for prior authorization






Flo-Pred 16.7 (15) mg/5 ml suspension – Implemented 07/08/2011
Millipred 5 mg Dose Pack – Implemented 01/18/2011
Millipred 5 mg tablet – Implemented 01/18/2011
Millipred 10 mg/5 ml solution – Implemented 04/21/2009
Orapred ODT tablet – Implemented 08/17/2010
Veripred 20 mg/5 ml solution – Implemented 04/21/2009
Link to Memorandum: Millipred Tablets, Dose Pack
Link to Memorandum: Millipred Solution
Link to Memorandum: Orapred ODT
Link to Memorandum: Veripred
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Prednisone (Rayos DR)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization



Rayos DR 1mg
Rayos DR 2mg
Rayos DR 5mg
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Propafenone SR (Rythmol SR)
(Implemented 04/08/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria

>/= 90 days of Propafenone SR therapy in the past 120 days
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Proton Pump Inhibitors
(Implemented 08/17/2010)
Prescribers may request an override for nonpreferred drugs by calling the
UAMS College of Pharmacy Evidence-Based Prescription Drug Program
Help Desk at 1-866-250-2518 (toll-free) or 501-526-4200 (local).
Preferred agents with criteria


Omeprazole 20mg capsule (Rx Prilosec)
Pantoprazole sodium (Protonix)
Nonpreferred agents









Dexlansoprazole (Dexilant)
Esomeprazole magnesium capsule (Nexium)
Esomeprazole magnesium packet (Nexium Packet)
Esomeprazole magnesium/Naproxen tablet (Vimovo)
Esomeprazole strontium capsule
Omeprazole 10mg, 40mg capsule (Rx Prilosec)
Omeprazole suspension (Prilosec Suspension)
Omeprazole/sodium bicarbonate (Zegerid)
Rabeprazole sodium (Aciphex)
Nonpreferred agents with criteria


Lansoprazole capsule (Prevacid capsule)
Lansoprazole solutab (Prevacid Solutab)
Approval criteria for preferred agents with criteria



Approve up to 93 days of proton pump inhibitor therapy per year for all
recipients age 15 months or older
Approve treatment beyond 93 days for recipients 15 months or older who
have a diagnosis in history for Zollinger-Ellison Syndrome, Barrett’s
esophagus, or an endoscopy (Appendix I) in the past 24 months
Approve treatment beyond 93 days for recipients 15 months or older who
have a diagnosis in history for Cystic Fibrosis, pancreatic insufficiency, or
pancreatic disease in the past 24 months
Approval criteria for nonpreferred agents with criteria


Prevacid capsules
 < 1 year of age
Prevacid solutabs
 < 7 years of age
 Seven years of age and older with documented history of NPO
(Appendix A) within past 365 days.
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Denial criteria



Prevacid capsules
 > 1 year of age
Prevacid solutabs
 ≥ 7 years of age
 No documented history of NPO (Appendix A) within past 365 days
All Proton Pump Inhibitors
 > 93 days of PPI therapy in the past 365 days for recipients 15
months or older, unless there is a diagnosis in history for ZollingerEllison Syndrome, Barrett’s esophagus, Cystic Fibrosis, pancreatic
insufficiency, pancreatic disease, or an endoscopy (Appendix I) in
the past 24 months
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Pyridostigmine Timespan (Mestinon Timespan)
(Implemented 04/08/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria

>/= 90 days of Pyridostigmine ER therapy in the past 120 days
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Calcitriol (Vectical), Calcipotriene (Dovonex, Sorilux)
(Implemented 06/19/2006)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drug
Dovonex
Sorilux
Vectical
Approval criteria



Diagnosis of psoriasis in Medicaid history in previous 365 days
2 paid claims of a topical corticosteroid in previous 27-60 days
At least one paid claim for a topical corticosteroid must be from the very
high potency category
Approval criteria



Diagnosis of psoriasis in Medicaid history in previous 365 days
The incoming claim matches claim in history in the previous 45 days for
Vectical, Dovonex, Sorilux
At least two claims of a topical corticosteroid in previous 60 days in drug
claim history with at least one topical corticosteroid claim 14-60 days back
in history
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Quinine Sulfate (Qualaquin)
(Implemented 06/27/2007)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria




Submitted ICD-9 diagnosis of uncomplicated plasmodium falciparum
malaria in the previous 6 months,
AND
Concurrent therapy with seven days of Tetracycline, OR
Concurrent therapy with seven days Doxycycline, OR
Concurrent therapy with seven days Clindamycin.
Denial criteria
Absence of approval criteria
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Raloxifene (Evista)
(Implemented 08/21/2010)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria




Diagnosis of postmenopause in the previous 2 years, AND
o Diagnosis of breast cancer in the previous 2 years
OR
Diagnosis of postmenopause in the previous 2years, AND
Diagnosis of osteoporosis in the previous 2 years, AND
o Diagnosis of esophageal strictures in the previous 2 years , OR
o Diagnosis of esophageal achalasia in the previous 2 years
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Ranolazine (Ranexa)
(Implemented 10/18/2006)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Denial criteria
Diagnosis of hepatic impairment in the last 12 months
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Regorafenib (Stivarga) 40mg Tablet
(Implemented 03/19/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Stivarga
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Respiratory Syncytial Virus (RSV) Medications
(Implemented 01/01/1999)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Synagis
PA form
PA Forms available during RSV season at www.medicaid.state.ar.us
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Rifaximin 550mg Tablets (Xifaxan)
(Implemented 09/28/2010)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria

Diagnosis of Hepatic Encephalopathy in the previous 2 years.
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Rilonacept Injection (Arcalyst)
(Implemented 07/09/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that requires manual review for prior authorization

Arcalyst Injection
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Riociguat Tablet (Adempas)
(Implemented 03/18/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization





Adempas 0.5 mg Tablet
Adempas 1 mg Tablet
Adempas 1.5 mg Tablet
Adempas 2 mg Tablet
Adempas 2.5 mg Tablet
Additional criteria

Quantity edits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Rivaroxaban 10mg Tablet (Xarelto)
(Implemented 04/17/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria




One claim of up to 31 tablets of 10 mg will be allowed at POS for inferred
surgery prophylaxis, AND
One paid claim for Xarelto 10 mg will be allowed once every 186 days for
inferred surgery prophylaxis, AND
There are no paid claims for others strengths of Xarelto® in the previous 6
months of Medicaid drug history, AND
No therapeutic duplication with overlapping days’ supply allowed between
Xarelto 10 mg claim and a claim for a Low Molecular Weight heparin
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Rivaroxaban 15mg, 20mg Tablet, Starter Pack (Xarelto)
(Implemented 04/17/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria



No Therapeutic duplication allowed between different strengths of Xarelto
One (1) therapeutic duplication with overlapping days’ supply will be allowed
once per 186 days for inferred change in therapy between an Xarelto® claim
and any of the following: a Pradaxa® claim, a warfarin claim, OR a Eliquis®
claim, AND
The Xarelto® claim and the warfarin claim, the Pradaxa® claim, or the
Eliquis® claim cannot have the same date of service.
Additional criteria
Quantity limits apply
Link to Memorandum
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Rivastigmine Solution (Exelon)
(Implemented 09/18/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval Exelon:
 Age > 50 years of age, AND
 Diagnosis of NPO in the Medicaid History
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Ropinirole XL (Requip XL)
(Implemented 03/19/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
 Diagnosis of Parkinson’s Disease in Medicaid history in previous 2 years
AND
 >/= 90 days of therapy of Ropinirole XL in the past 120 days
Link to Memorandum
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Rotigotine (Neupro) Patch
(Implemented 03/19/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria

Diagnosis of Parkinson’s Disease in Medicaid history in previous 2 years
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Rosacea Treatment
(Implemented 06/19/2006)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drug
Finacea 15% Gel
Metrogel 1% Topical
Mirvaso 0.33% Gel
Noritate 1% Cream
Approval criteria


Diagnosis of rosacea in Medicaid history in previous 2 years
2 paid claims for generic metronidazole 0.75% cream, gel, or lotion in the
previous 27-60 days
Denial criteria

History of acne vulgaris in the last 60 days
Drugs that do not require a PA
o Metronidazole 0.75% Topical Cream [MetroCream 0.75%]
o Metronidazole 0.75% Topical Gel [Metrogel 0.75%]
o Metronidazole 0.75% Topical Lotion [MetroLotion 0.75%]
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Ruxolitinib Tablets (Jakafi)
(Implemented 04/17/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
No Therapeutic duplication allowed between different strengths of Jakafi
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Sapropterin Dihydrochloride (Kuvan)
(Implemented 04/12/2011)
Prescribers are required to fax a letter of medical necessity and include all
supporting documentation for manual review to 501-683-4124.
Drugs that requires manual review for prior authorization

Kuvan
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Sedative Hypnotics
(Implemented 06/19/2006)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drug
Estazolam (Prosom)
Flurazepam (Dalmane)
Quazepam (Doral)
Temazepam (Restoril)
Triazolam (Halcion)
Denial criteria
Therapeutic duplication with any of the following sedative hypnotic
 Estazolam (Prosom)
 Eszopiclone (Lunesta)*
 Flurazepam (Dalmane)
 Quazepam (Doral)
 Ramelteon (Rozerem)*
 Temazepam (Restoril)
 Triazolam (Halcion)
 Zaleplon (Sonata)*
 Zolpidem (Ambien)*
 Zolpidem (Zolpimist)*
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Serostim
(Implemented 10/18/2006)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that requires manual review for prior authorization

Serostim
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Serotonin 5-HT 1 Receptor Agonists
(Implemented 07/01/2010)
Prescribers may request an override for nonpreferred drugs by calling the
UAMS College of Pharmacy Evidence-Based Prescription Drug Program
Help Desk at 1-866-250-2518 (toll-free) or 501-526-4200 (local).
Preferred agents with criteria







Sumatriptan 4mg/0.5ml kit refill (Imitrex)
Sumatriptan 5mg nasal spray (Imitrex)
Sumatriptan 6mg/0.5ml kit refill (Imitrex)
Sumatriptan 6mg/0.5ml kit syringe (Imitrex)
Sumatriptan 6mg/0.5ml vial (Imitrex)
Sumatriptan 20mg nasal spray (Imitrex)
Sumatriptan succinate tablet (Imitrex)
Nonpreferred agents












Almotriptan malate (Axert)
Eletriptan HBr (Relpax)
Frovatriptan succinate (Frova)
Naratriptan HCl (Amerge)
Rizatriptan benzoate (Maxalt)
Sumatriptan 4mg/0.5ml needle free injection (Sumavel Dosepro)
Sumatriptan 4mg/0.5ml syringe (Non MAC’d)
Sumatriptan 4mg/0.5ml vial
Sumatriptan 6mg/0.5ml needle free injection (Sumavel Dosepro)
Sumatriptan 6mg/0.5ml syringe (Non MAC’d)
Sumatriptan succinate/naproxen sodium (Treximet)
Zolmitriptan (Zomig)
Nonpreferred agents with criteria
Rizatriptan benzoate disintegrating (Maxalt MLT)
Approval criteria for preferred agents with criteria
Preferred Injection
 Any serotonin 5-HT 1 receptor antagonist within past 365 days
Approval criteria for nonpreferred agents with criteria:
Maxalt MLT tablet
 Any preferred serotonin 5-HT 1 receptor antagonist, Maxalt tablet, or
Maxalt MLT tablet within past 365 days
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Denial criteria for all agents:
Therapeutic duplication of any serotonin 5-HT 1 receptor agonist
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Sildenafil (Revatio)
(Implemented 10/11/2005)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria



Diagnosis of pulmonary heart disease in the last 365 days, OR
Diagnosis of persistent fetal circulation in the last 365 days, OR
Diagnosis of chronic respiratory disease arising in the perinatal period in
the last 365 days
Denial criteria



One of the following diagnoses in the last 180 days:
o Cavernosal fibros, OR
o Hypotension, OR
o Leukemia, OR
o Life-threatening arrhythmia, OR
o Malignant hypertension, OR
o Multiple myeloma, OR
o Myocardial infarction, OR
o Peyronie’s disease, OR
o Retinitis pigmentosa, OR
o Sickle cell disease, OR
o Stroke, OR
o Unstable angina
History of any of the following in the last 45 days:
o Alpha-adrenergic blockers
o Nitrates
o Tamsulosin
Concurrent use of any the following:
o Indinavir
o Lopinavir-ritonavir
o Ritonavir
Additional criteria
Quantity limits apply
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Siltuximab vial (Sylvant)
(Implemented 09/23/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Sylvant
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Sinecatechins (Veregen ointment 15%)
(Implemented 06/19/2008)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria


Diagnosis for of Condyloma Acuminanta (commonly known as external
genital or perianal warts) within the past two months, AND
≤ 124 days of Veregen therapy in the past 365 days
Additional criteria
Limited to 18 years and older
Max quantity per claim = 30 grams
Limited to 60 grams per 365 days
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Skeletal Muscle Relaxants
(Implemented 03/20/2006)
Prescribers may request an override for nonpreferred drugs by calling the
UAMS College of Pharmacy Evidence-Based Prescription Drug Program
Help Desk at 1-866-250-2518 (toll-free) or 501-526-4200 (local).
Preferred agents



Chlorzoxazone 500 mg tablet (Parafon)
Cyclobenzaprine HCl 10mg tablet (Flexeril)
Methocarbamol (Robaxin)
Preferred agents with criteria


Baclofen tablet (Lioresal)
Tizanidine HCl tablet (Zanaflex Tablet)
Nonpreferred agents











Carisoprodol (Soma)
Carisoprodol/Aspirin (Soma Compound)
Carisoprodol/Aspirin/Codeine (Soma Compound w/ Codeine)
Chlorzoxazone 375 mg, 750 mg tablet (Lorzone)
Cyclobenzaprine HCl 5mg, 7.5mg tablet (Flexeril, Fexmid)
Cyclobenzaprine HCl extended-release capsule (Amrix)
Dantrolene sodium (Dantrium)
Metaxalone (Skelaxin)
Orphenadrine citrate (Norflex)
Orphenadrine/aspirin/caffeine (Norgesic)
Tizanidine HCL capsule (Zanaflex Capsule)
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Approval criteria for preferred agents with criteria
Baclofen tablet (Lioresal) and tizanidine HCl tablet (Zanaflex tablet)
One of the following diagnoses:
ICD-9
333.7
340
342.1
343
Description
Symptomatic torsion
dystonia
Multiple sclerosis
Spastic hemiplegia
Infantile cerebral palsy
ICD-9
433.x
1
767.4
781.0
806
345.6
430
Infantile spasms
Subarachnoid hemorrhage
851
900
431
432
Intracerebral hemorrhage
Other and unspecified
intracranial hemorrhage
907.2
952
Top of the document
Description
Occlusion and stenosis of precerebral
arteries with cerebral infarction
Injury to spine and spinal cord
Abnormal involuntary movements
Fracture of vertebral column with spinal
cord injury
Cerebral laceration and contusion
Injury to blood vessels of head and
neck
Late effect of spinal cord injury
Spinal cord injury without evidence of
spinal bone injury
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Sodium chloride 7% Inhalation Solution (Hyper-Sal 7%)
(Implemented 05/24/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria

Diagnosis of cystic fibrosis within the past three years
Additional criteria
Quantity limits apply
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Sodium Oxybate (Xyrem)
(Implemented 10/10/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria

Diagnosis for Narcolepsy with Cataplexy in past two years
Denial criteria



Claim for a Sedative/Hypnotic Agent in previous thirty days
Diagnosis of Alcohol Abuse in the previous eighteen months
Diagnosis of Fibromyalgia in the previous two years
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Somatropin (Genotropin)
(Implemented 01/24/2007)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
Must meet one of the following five criteria:
Criterion 1:
 Age < 18 years of age, AND
 Submitted diagnosis of Prader-Willi Syndrome (PWS) in the last two years
Criterion 2:
 Age < 18 years of age, AND
 Submitted diagnosis of Turner Syndrome in the last two years
Criterion 3:
 Age < 18 years of age, AND
 Submitted ICD-9 diagnosis in the last two years:
o Pituitary dwarfism, OR
o Panhypopituitarism, OR
o Iatrogenic pituitary disorder, OR
o Unspecified disorder of the pituitary gland, OR
o Craniopharyngioma, OR
o Septo-optic dysplasia
AND all of the following:
 Growth Hormone Deficiency (GHD) confirmed by provocative GH
Stimulation Testing, AND
 MRI or CT scan within the past two years, AND
 Documented test for hypothyroidism (T3 or T4 level) within the past two
years, AND
 Recipients > 14 years of age: X-ray of the femur or finger within 365 days
Criterion 4:
 Age > 18 years of age, AND
 Submitted ICD-9 diagnosis for one of the following in the last two years:
o Pituitary dwarfism, OR
o Iatrogenic pituitary disorder, OR
o Unspecified disorder of the pituitary gland
AND
o GHD confirmed by provocative GH stimulation testing within
the last two years.
Criterion 5:
 Age > 18 years of age, AND
 Submitted ICD-9 diagnosis of panhypopituitarism, AND
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria


Two of the following appropriate replacement therapies (five paid claims in
the past 180 days):
o Thyroid hormones
o Hydrocortisone
o Estrogen
o Testosterone, OR
GHD confirmed by GH Stimulation testing or IGF-1 within the past two
years
Denial criteria


History of any of the following diagnoses:
o Age > 65 years of age
o History of malignancy in the past 365 days
o History of renal transplant in the past 365 days
o Pregnancy
History of Prader-Willi Syndrome concurrently with any of the following
diagnoses:
o Severe obesity
o Sleep apnea
o History of severe respiratory impairment
Growth Hormone Continuation Criteria
Point-of-sale continuation criteria have been added to the current growth
hormone criteria for certain diagnoses. The following point-of-sale continuation
criteria were implemented on Nov. 16, 2011:

For recipients < age 13 years for females and < age 14 for males with a
billed diagnosis of pituitary dwarfism within the previous 2 years AND a
paid claim in Medicaid history for growth hormone in the previous 6
months.

For recipients < age 18 years with a billed diagnosis of
panhypopituitarism, Turner’s syndrome, Prader-Willi syndrome OR septioptic dysplasia within the previous 2 years AND a paid claim in Medicaid
history for growth hormone within the previous 6 months.
Link to Memorandum
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Somatropin (Humatrope)
(Implemented 01/24/2007)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
Must meet one of the following four criteria:
Criterion 1:
 Age < 18 years of age, AND
 Submitted diagnosis of Turner Syndrome in the last two years
Criterion 2:
 Age < 18 years of age, AND
 Submitted ICD-9 diagnosis in the last two years of:
o Pituitary dwarfism, OR
o Panhypopituitarism, OR
o Iatrogenic pituitary disorder, OR
o Unspecified disorder of the pituitary gland, OR
o Craniopharyngioma, OR
o Septo-optic dysplasia
AND all of the following in the last two years:
o Growth Hormone Deficiency (GHD) confirmed by
provocative GH Stimulation Testing, AND
o MRI or CT scan within the past two years, AND
o Documented test for hypothyroidism (T3 or T4 level) within
the past two years, AND
o Recipients > 14 years of age: X-ray of the femur or finger
within 365 days
Criterion 3:
 Age > 18 years of age, AND
 Submitted ICD-9 diagnosis for one of the following in the last two years:
o Pituitary dwarfism OR
o Iatrogenic pituitary disorder OR
o Unspecified disorder of the pituitary gland
AND
o GHD confirmed by provocative GH stimulation testing within
the last two years.
Criterion 4:
 Age > 18 years of age, AND
 Submitted ICD-9 diagnosis of panhypopituitarism, AND
 Two of the following appropriate replacement therapies (five claims in the
past 180 days):
o Thyroid hormones
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
o
o
o
o
Hydrocortisone
Estrogen
Testosterone, OR
GHD confirmed by GH stimulation testing or IGF-1 within the
past two years
Denial criteria

History of any of the following diagnoses:
o Age > 65 years of age
o History of malignancy in the past 365 days
o History of renal transplant in the past 365 days
o Pregnancy
Growth Hormone Continuation Criteria
Point-of-sale continuation criteria have been added to the current growth
hormone criteria for certain diagnoses. The following point-of-sale continuation
criteria were implemented on Nov. 16, 2011:

For recipients < age 13 years for females and < age 14 for males with a
billed diagnosis of pituitary dwarfism within the previous 2 years AND a
paid claim in Medicaid history for growth hormone in the previous 6
months.

For recipients < age 18 years with a billed diagnosis of
panhypopituitarism, Turner’s syndrome, Prader-Willi syndrome OR septioptic dysplasia within the previous 2 years AND a paid claim in Medicaid
history for growth hormone within the previous 6 months.
Link to Memorandum
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Somatropin (Norditropin and Saizen)
(Implemented 01/24/2007)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
Must meet one of the following three criteria:
Criterion 1:
 Age < 18 years of age, AND
 Submitted ICD-9 diagnosis in the last two years:
o Pituitary dwarfism OR
o Panhypopituitarism OR
o Iatrogenic pituitary disorder OR
o Unspecified disorder of the pituitary gland OR
o Craniopharyngioma OR
o Septo-optic dysplasia
AND all of the following in the last two years:
o Growth Hormone Deficiency (GHD) confirmed by
provocative GH stimulation testing, AND
o MRI or CT scan within the past 2 years, AND
o Documented test for hypothyroidism (T3 or T4 level) within
the past two years, AND
o Recipients > 14 years of age: X-ray of the femur or finger
within 365 days
Criterion 2:
 Age > 18 years of age, AND
 Submitted ICD-9 diagnosis for one of the following in the last two years:
o Pituitary dwarfism, OR
o Iatrogenic pituitary disorder, OR
o Unspecified disorder of the pituitary gland
AND
o GHD confirmed by provocative GH stimulation testing within
the last two years.
Criterion 3:
 Age > 18 years of age, AND
 Submitted ICD-9 diagnosis of panhypopituitarism, AND
 Two of the following appropriate replacement therapies (five claims in the
past 180 days):
o Thyroid hormones
o Hydrocortisone
o Estrogen
o Testosterone, OR
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
o GHD confirmed by GH stimulation testing or IGF-1 within the
past two years,
Denial criteria




Age > 65 years of age
History of malignancy in the past 365 days
History of renal transplant in the past 365 days
Pregnancy
Growth Hormone Continuation Criteria
Point-of-sale continuation criteria have been added to the current growth
hormone criteria for certain diagnoses. The following point-of-sale continuation
criteria were implemented on Nov. 16, 2011:

For recipients < age 13 years for females and < age 14 for males with a
billed diagnosis of pituitary dwarfism within the previous 2 years AND a
paid claim in Medicaid history for growth hormone in the previous 6
months.

For recipients < age 18 years with a billed diagnosis of
panhypopituitarism, Turner’s syndrome, Prader-Willi syndrome OR septioptic dysplasia within the previous 2 years AND a paid claim in Medicaid
history for growth hormone within the previous 6 months.
Link to Memorandum
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Somatropin (Nutropin)
(Implemented 01/24/2007)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
Must meet one of the following six criteria:
Criterion 1:
 Age <18 years of age, AND
 Submitted diagnosis of Turner Syndrome in the last two years
Criterion 2:
 Age < 18 years of age, AND
 Submitted diagnosis of chronic renal Insufficiency
Criterion 3:
 Age < 18 years of age, AND
 Submitted diagnosis of end-stage renal disease awaiting transplantation
Criterion 4:
 Age < 18 years of age, AND
 Submitted ICD-9 diagnosis in the last two years:
o Pituitary dwarfism, OR
o Panhypopituitarism, OR
o Iatrogenic pituitary disorder, OR
o Unspecified disorder of the pituitary gland, OR
o Craniopharyngioma, OR
o Septo-optic dysplasia
AND all of the following in the last two years:
o Growth Hormone Deficiency (GHD) confirmed by
provocative GH stimulation testing, AND
o MRI or CT scan within past two years, AND
o Documented test for hypothyroidism (T3 or T4 level) within
past 2 years, AND
o Recipients > 14 years of age: X-ray of the femur or finger
within 365 days
Criterion 5:
 Age > 18 years of age, AND
 Submitted ICD-9 diagnosis for one of the following in the last two years:
o Pituitary dwarfism, OR
o Iatrogenic pituitary disorder, OR
o Unspecified disorder of the pituitary gland
AND
o GHD confirmed by provocative GH stimulation testing within
the last two years.
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Criterion 6:
 Age > 18 years of age, AND
 Submitted ICD-9 diagnosis of panhypopituitarism, AND
 Two of the following appropriate replacement therapies (five claims in the
past 180 days):
o Thyroid hormones
o Hydrocortisone
o Estrogen
o Testosterone, OR
o GHD confirmed by GH stimulation testing or IGF-1 within the
past two years.
Denial criteria




Age > 65 years of age
History of malignancy in the past 365 days
History of renal transplant in the past 365 days
Pregnancy
Growth Hormone Continuation Criteria
Point-of-sale continuation criteria have been added to the current growth
hormone criteria for certain diagnoses. The following point-of-sale continuation
criteria were implemented on Nov. 16, 2011:

For recipients < age 13 years for females and < age 14 for males with a
billed diagnosis of pituitary dwarfism within the previous 2 years AND a
paid claim in Medicaid history for growth hormone in the previous 6
months.

For recipients < age 18 years with a billed diagnosis of
panhypopituitarism, Turner’s syndrome, Prader-Willi syndrome OR septioptic dysplasia within the previous 2 years AND a paid claim in Medicaid
history for growth hormone within the previous 6 months.
Link to Memorandum
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Somatropin (Omnitrope)
(Implemented 01/24/2007)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
Must meet one of the following six criteria:
Criterion 1:
 Age < 18 years of age, AND
 Submitted diagnosis of Prader-Willi Syndrome (PWS) in the last two years
Criterion 2:
 Age < 18 years of age, AND
 Submitted diagnosis of Turner Syndrome in the last two years
Criterion 3:
 Age < 18 years of age, AND
 Submitted diagnosis of chronic renal insufficiency
Criterion 4:
 Age < 18 years of age, AND
 Submitted diagnosis of end-stage renal disease awaiting transplantation
Criterion 5:
 Age < 18 years of age, AND
 Submitted ICD-9 diagnosis in the last two years:
o Pituitary dwarfism, OR
o Panhypopituitarism, OR
o Iatrogenic pituitary disorder, OR
o Unspecified disorder of the pituitary gland OR
o Craniopharyngioma, OR
o Septo-optic dysplasia
AND all of the following in the last two years:
o Growth Hormone Deficiency (GHD) confirmed by
provocative GH stimulation testing, AND
o MRI or CT scan within past 2 years, AND
o Documented test for hypothyroidism (T3 or T4 level) within
past two years, AND
o Recipients > 14 years of age: X-ray of the femur or finger
within 365 days
Criterion 6:
 Age >18 years of age, AND
 Submitted ICD-9 diagnosis for one of the following in the last two years:
o Pituitary dwarfism, OR
o Iatrogenic pituitary disorder, OR
o Unspecified disorder of the pituitary gland
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
AND
o GHD confirmed by provocative GH stimulation testing within
the last two years.
Criterion 7:
 Age > 18 years of age, AND
 Submitted ICD-9 diagnosis of panhypopituitarism, AND
 Two of the following appropriate replacement therapies (five claims in the
past 180 days):
o Thyroid hormones
o Hydrocortisone
o Estrogen
o Testosterone, OR
o GHD confirmed by GH stimulation testing or IGF-1 within the
past two years
Denial criteria




Age > 65 years of age
History of malignancy in the past 365 days
History of renal transplant in the past 365 days
Pregnancy
Growth Hormone Continuation Criteria
Point-of-sale continuation criteria have been added to the current growth
hormone criteria for certain diagnoses. The following point-of-sale continuation
criteria were implemented on Nov. 16, 2011:

For recipients < age 13 years for females and < age 14 for males with a
billed diagnosis of pituitary dwarfism within the previous 2 years AND a
paid claim in Medicaid history for growth hormone in the previous 6
months.

For recipients < age 18 years with a billed diagnosis of
panhypopituitarism, Turner’s syndrome, Prader-Willi syndrome OR septioptic dysplasia within the previous 2 years AND a paid claim in Medicaid
history for growth hormone within the previous 6 months.
Link to Memorandum
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Somatropin (Tev-tropin)
(Implemented 01/24/2007)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
Must meet one of the following criteria:
 Age < 18 years of age, AND
 Submitted ICD-9 diagnosis in the last two years:
o Pituitary dwarfism, OR
o Panhypopituitarism, OR
o Iatrogenic pituitary disorder, OR
o Unspecified disorder of the pituitary gland, OR
o Craniopharyngioma, OR
o Septo-optic dysplasia
AND all of the following in the last two years:
o Growth Hormone Deficiency (GHD) confirmed by
provocative GH stimulation testing, AND
o MRI or CT scan within the past 2 years, AND
o Documented test for hypothyroidism (T3 or T4 level) within
the past two years, AND
o Recipients > 14 years of age: X-ray of the femur or finger
within 365 days
Denial criteria




Age > 65 years of age
History of malignancy in the past 365 days
History of renal transplant in the past 365 days
Pregnancy
Growth Hormone Continuation Criteria
Point-of-sale continuation criteria have been added to the current growth
hormone criteria for certain diagnoses. The following point-of-sale continuation
criteria were implemented on Nov. 16, 2011:

For recipients < age 13 years for females and < age 14 for males with a
billed diagnosis of pituitary dwarfism within the previous 2 years AND a
paid claim in Medicaid history for growth hormone in the previous 6
months.
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria

For recipients < age 18 years with a billed diagnosis of
panhypopituitarism, Turner’s syndrome, Prader-Willi syndrome OR septioptic dysplasia within the previous 2 years AND a paid claim in Medicaid
history for growth hormone within the previous 6 months.
Link to Memorandum
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Somatropin (Zorbtive)
(Implemented 01/24/2007)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
Criterion 6:
 Age > 18 years of age, AND
 Submitted ICD-9 diagnosis of short bowel syndrome
Additional criteria
Quantity limits apply
Denial criteria




Age > 65 years of age
History of malignancy in the past 365 days
History of renal transplant in the past 365 days
Pregnancy
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Spinosad 0.9% Topical Suspension (Natroba)
(Implemented 06/21/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Natroba
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Sucralfate Suspension (Carafate)
(Implemented 10/11/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria


< 6 years of age, OR
NPO (Appendix A)
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Sulfamethoxazole-Trimethoprim 800-160/20ml U.D.
Cup
(Implemented 04/08/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
Currently LTC
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Sunitinib (Sutent) Capsule
(Implemented 01/13/2015)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Sutent
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Tacrolimus (Astagraf XL)
(Implemented 12/10/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Astagraf XL
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Tacrolimus (Protopic)
(Implemented 03/12/2007)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria




No therapeutic duplication with other strengths of Tacrolimus (Protopic),
AND
No therapeutic duplication Pimecrolimus (Elidel), AND
At least two paid Medicaid drug claims of topical corticosteroid agents,
each containing a different drug entity, AND
At least one of the claims for the topical corticosteroid being at least
medium potency or higher filled in the previous 14-45 day period.
Denial criteria





History of Psoriasis in previous two years
Therapeutic duplication with other strengths of tacrolimus (Protopic)
Therapeutic duplication with pimecrolimus (Elidel)
No claim for at least two topical corticosteroids in Medicaid history
No claim for a medium potency or higher topical corticosteroid in the
previous 14-45 day period.
Additional criteria


Tacrolimus 0.03%
o Age > 2 years of age
o Quantity limits apply
Tacrolimus 0.1%
o Age > 16 years of age
o Quantity limits apply
Denial criteria



Tacrolimus 0.03%
o Therapeutic duplication with pimecrolimus (Elidel)
o Therapeutic duplication with tacrolimus (Protopic) 0.1%
Tacrolimus 0.1%
o Therapeutic duplication with pimecrolimus (Elidel)
o Therapeutic duplication with tacrolimus (Protopic) 0.03%
History of Psoriasis in previous two years
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria


No claim for at least two topical corticosteroids in Medicaid history
No claim for a medium potency or higher topical corticosteroid in the
previous 14-45 day period.
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Tadalafil (Adcirca)
(Implemented 09/15/2009)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria



Diagnosis of pulmonary heart disease in the last 365 days, OR
Diagnosis of persistent fetal circulation in the last 365 days, OR
Diagnosis of chronic respiratory disease arising in the perinatal period in
the last 365 days
Denial criteria



One of the following diagnoses in the last 180 days:
o Cavernosal fibros, OR
o Hypotension, OR
o Leukemia, OR
o Life-threatening arrhythmia, OR
o Malignant hypertension, OR
o Multiple myeloma, OR
o Myocardial infarction, OR
o Peyronie’s disease, OR
o Retinitis pigmentosa, OR
o Sickle cell disease, OR
o Stroke, OR
o Unstable angina
History of any of the following in the last 45 days:
o Alpha-adrenergic blockers
o Tamsulosin
Concurrent use of any the following:
o Indinavir
o Lopinavir-ritonavir
o Ritonavir
Additional criteria
Quantity limits apply
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Tamoxifen 10mg/5ml Oral Solution (Soltamox)
(Implemented 03/19/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Soltamox
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Targeted Immune Modulators
(Implemented 10/17/2007)
Prescribers may request an override for nonpreferred drugs by calling the
UAMS College of Pharmacy Evidence-Based Prescription Drug Program
Help Desk at 1-866-250-2518 (toll-free) or 501-526-4200 (local).
Preferred agents with criteria



Adalimumab (Humira)
Cetrolizumab (Cimzia)
Etanercept (Enbrel)
Nonpreferred agents








Abatacept (Orencia)
Anakinra (Kineret)
Apremilast (Otezla)
Golimumab (Simponi)
Infliximab (Remicade)
Ustekinumab (Stelara)
Tocilizumab (Actemra)
Tofacitinib (Xeljanz)
Approval criteria for preferred agents with criteria
Approval criteria for Cimzia
Must meet one of the following five criteria:
 Criterion 1:
 Age ≥ 18, AND
 Submitted ICD-9 diagnosis for Crohn’s disease or regional enteritis (Table
5) in the past two years, AND
 Submitted ICD-9 diagnosis for fistula in the past 730 days (Table 5), AND
 Maximum of 1 Cimzia Starter Kit every 2 years or 1 syringe kit or 1 vial kit
every 23 days
 Criterion 2:
 Age ≥18, AND
 Submitted ICD-9 diagnosis of Crohn’s disease or regional enteritis (Table
5) in the past two years, AND
 ≥180 days of drug therapy in the past 365 days with any of the following:
systemic glucocorticoid AND mesalamine therapy, mercaptopurine, or
azathioprine, AND
 Maximum of 1 Cimzia Starter Kit every 2 years or 1 syringe kit or 1 vial kit
every 23 days
 Criterion 3:
 Age ≥18, AND
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Submitted ICD-9 diagnosis of Crohn’s disease or regional enteritis (Table
5) in the past two years, AND
 Paid drug claim for cetrolizumab (Cimzia) in the past 45 days, AND
 Maximum of 1 syringe kit or 1 vial kit every 23 days
Criterion 4:
 Age ≥18, AND
 Submitted ICD-9 diagnosis of rheumatoid arthritis (Table 5) in the past two
years, AND
 ≥6 claims of drug therapy in the past 365 days with any of the following:
gold compounds, hydroxychloroquine, penicillamine, methotrexate,
azathioprine, sulfasalazine, or leflunomide, AND
 Maximum of 1 Cimzia Starter Kit every 2 years or 1syringe kit or 1 vial kit
every 23 days
Criterion 5:
 Submitted ICD-9 diagnosis of rheumatoid arthritis (Table 5) in the past two
years, AND
 Paid Drug claim for cetrolizumab (Cimzia) in the past 45 days (signifying
above criteria previously met), AND
 Maximum of 1 syringe kit or 1 vial kit every 23 days
Criterion 6:
 Submitted ICD-9 diagnosis of psoriatic arthropathy (Table 5) in the past
two years, AND
 Age ≥18, AND
 ≥6 claims of drug therapy in the past 365 days with any of the following:
gold compounds, hydroxychloroquine, penicillamine, methotrexate,
azathioprine, sulfasalazine, or leflunomide, AND
 Maximum of 1 Cimzia Starter Kit every 2 years or 1syringe kit or 1 vial kit
every 23 days
Criterion 5:
 Submitted ICD-9 diagnosis of psoriatic arthropathy (Table 5) in the past
two years, AND
 Age ≥18, AND
 Paid Drug claim for cetrolizumab (Cimzia) in the past 45 days (signifying
above criteria previously met), AND
 Maximum of 1 syringe kit or 1 vial kit every 23 days





Approval criteria for Enbrel
Must meet one of the following six criteria:
 Criterion 1:
 Submitted ICD-9 diagnosis of psoriasis (Table 5) in the past two years,
AND
 Age > 17, AND
 Paid Drug claim for etanercept (Enbrel) in the past 45 days (signifying
above criteria previously met)
 Criterion 2:
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria







Submitted diagnosis of psoriasis (Table 5) in the past two years, AND
Age > 17, AND
During days 180 to 395 days ago, a total of > 180 days of topical drug
therapy with: anthralin, calcipotriene, corticosteroids, or tazarotene in past
395 days, AND
 During days 1 to 210 ago, a total of > 180 days of systemic drug therapy
with: cyclosporine, methotrexate, or acitretin, AND
 Topical drug therapy trial occurred before systemic drug therapy
Criterion 3:
Submitted ICD-9 diagnosis of ankylosing spondylosis (Table 5) in the past
two years
Criterion 4:
 Submitted ICD-9 diagnosis of rheumatoid arthritis (Table 5) or psoriatic
arthropathy (Table 5) in the past two years, AND
 >180 days of drug therapy in the past 365 days with any of the following:
gold compounds, hydroxychloroquine, penicillamine, methotrexate,
azathioprine, sulfasalazine, or leflunomide
Criterion 5:
 Submitted ICD-9 diagnosis of rheumatoid arthritis (Table 5) or psoriatic
arthropathy (Table 5) in the past two years, AND
 Paid Drug claim for etanercept (Enbrel) in the past 45 days (signifying
above criteria previously met)
Criterion 6:
 Submitted ICD-9 diagnosis of rheumatoid arthritis (Table 5) in the past two
years, AND
 Age < 18
Approval criteria for Humira
Must meet one of the following eight criteria:
 Criterion 1:
 Submitted ICD-9 diagnosis of ankylosing spondylosis (Table 5) in the past
two years
 Criterion 2:
 Submitted ICD-9 diagnosis for rheumatoid arthritis (Table 5) or psoriatic
arthropathy (Table 5) in the past two years, AND
 One of the following :
 > Six claims for any of the following in the past 365 days: gold
compounds, hydroxychloroquine, penicillamine, methotrexate,
azathioprine, sulfasalazine, or leflunomide, OR
 Paid Drug claim for adalimumab (Humira) in the past 45 days
(signifying above criteria previously met)
 Criterion 3:
 Age > 18 years, AND
 Submitted ICD-9 diagnosis code for Crohn’s disease (Table 5) or regional
enteritis (Table 5) in the past two years, AND
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria





 Submitted ICD-9 diagnosis code for fistula (Table 5) in the past two years
Criterion 4:
 Age > 18 years, AND
 Submitted ICD-9 diagnosis code for Crohn’s disease (Table 5) or regional
enteritis (Table 5) in the past two years, AND
 > 180 days drug therapy of one of the following regimens in the past 365
days:
 concurrent systemic glucocorticoid AND mesalamine therapy, OR
 mercaptopurine, OR
 azathioprine
Criterion 5:
 Age > 18 years, AND
 Submitted ICD-9 diagnosis code for Crohn’s disease (Table 5) or regional
enteritis (Table 5) in the past two years, AND
 Drug claim for adalimumab (Humira) in the past 45 days (signifying
above criteria previously met)
Criterion 6:
 Submitted ICD-9 diagnosis of psoriasis (Table 5) in the past two years,
AND
 Age > 18, AND
 Paid drug claim for adalimumab (Humira) in the past 45 days (signifying
above criteria previously met)
Criterion 7:
 Submitted diagnosis of ICD-9 psoriasis (Table 5) in the past two years,
AND
 Age > 18, AND
 During days 180 to 395 days ago, a total of >180 days of topical drug
therapy with: anthralin, calcipotriene, corticosteroids, or tazarotene in past
395 days, AND
 During days 1 to 210 ago, a total of > 180 days of systemic drug therapy
with: cyclosporine, methotrexate, or acitretin, AND
 Topical drug therapy trial occurred before systemic drug therapy
Criterion 8:
 Submitted ICD-9 diagnosis of rheumatoid arthritis (Table 5) in the past two
years, AND
 Age < 18
Table 5 – Targeted immune modulator diagnoses
Drug
Cimzia
Cimzia
Cimzia
Cimzia
Cimzia
ICD-9
555
555
565.1
567.2
567.2
Description
Crohn's disease
Regional enteritis
Anal fistula
Peritonitis (acute) generalized
Peritoneal abscess
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Cimzia
Cimzia
Cimzia
Cimzia
Cimzia
Cimzia
Cimzia
Cimzia
Cimzia
Cimzia
Cimzia
Cimzia
Enbrel
Enbrel
Enbrel
Enbrel
Humira
Humira
Humira
Humira
Humira
Humira
Humira
Humira
Humira
Humira
Humira
Humira
Humira
Humira
Humira
Humira
Humira
Humira
Humira
Humira
567.2
567.2
567.3
567.3
567.3
567.3
567.8
567.8
567.8
569.8
696.0
714
696.0
696.1
714
720
555
555
556
565.1
567.2
567.2
567.2
567.3
567.3
567.3
567.3
567.3
567.8
567.8
567.9
569.8
696.0
696.1
714
720
Spontaneous bacterial peritonitis
Other suppurative peritonitis
Retroperitoneal infections
Psoas muscle abscess
Other retroperitoneal abscess
Other retroperitoneal infections
Choleperitonitis
Sclerosing mesenteritis
Other specified peritonitis
Fistula of intestine excluding rectum and anus
Psoriatic arthropathy
Rheumatoid arthritis and other inflammatory polyarthropathies
Psoriatic arthropathy
Other psoriasis
Rheumatoid arthritis and other inflammatory polyarthropathies
Ankylosing spondylosis
Crohn's disease
Regional enteritis
Ulcerative Colitis
Anal fistula
Peritonitis (acute) generalized
Peritoneal abscess
Spontaneous bacterial peritonitis
Other suppurative peritonitis
Retroperitoneal infections
Psoas muscle abscess
Other retroperitoneal abscess
Other retroperitoneal infections
Choleperitonitis
Sclerosing mesenteritis
Other specified peritonitis
Fistula of intestine excluding rectum and anus
Psoriatic arthropathy
Other psoriasis
Rheumatoid arthritis and other inflammatory polyarthropathies
Ankylosing spondylosis
Link to Memorandum: Humira
Link to Memorandum: Enbrel
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Tasimelteon Capsule (Hetlioz)
(Implemented 09/23/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Hetlioz Capsule
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Tavaborole 5% Topical Solution (Kerydin)
(Implemented 01/13/2015)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that do not require prior authorization


Itraconazole Capsule [Sporanox]
Terbinafine Tablet [Lamisil]
Drugs that require manual PA



Ciclopirox 8% Topical Solution [Penlac]
Efinaconazole 10% Topical Solution [Jublia]
Tavaborole 5% Topical Solution [Kerydin]
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Tazarotene Gel/Cream (Tazorac)
(Implemented 06/19/2006)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drug
Tazorac
Approval criteria (New Start)
 Diagnosis of psoriasis in Medicaid history in previous 365 days,
AND
 2 paid claims of a topical corticosteroid in previous 27-60 days,
AND
 At least one paid claim for a topical corticosteroid must be from the very
high potency category.
Approval criteria (Continuation Criteria)
 Diagnosis of psoriasis in Medicaid history in previous 365 days,
AND
 The incoming claim matches claim in history in the previous 45 days of
Tazorac,
AND
 At least two claims of a topical corticosteroid in previous 60 days in drug
claim history with at least one topical corticosteroid claim 14-60 days back
in history.
Denial criteria
History of acne vulgaris in the last 60 days
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Tedizolid (Sivextro)
(Implemented 01/13/2015)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria

No therapeutic duplication between a claim of the tablets and claim of the
vials within the same month
Additional criteria


Age >/= 18 years of age
Quantity Limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Teduglutide Vial (Gattex)
(Implemented 07/09/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Gattex
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Telithromycin (Ketek)
(Implemented 09/12/2007)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Denial criteria



Submitted ICD-9 diagnosis myasthenia gravis in the past 730 days.
Submitted ICD-9 diagnosis hepatitis in the past 730 days.
Submitted ICD-9 diagnosis hepatic impairment in the past 730 days.
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Temazepam 7.5mg and 22.5mg Capsule (Restoril)
(Implemented 07/09/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization


Temazepam 7.5mg capsule
Temazepam 22.5 mg capsule
Exceptions (Beneficiaries that do not require a Prior Authorization)

Temazepam 7.5mg capsule
 Long Term Care Beneficiaries
 Beneficiaries that are 65 years of age of older
*No PA required for requests for Temazepam 7.5mg Capsule for the Beneficiaries listed
above*
Approval criteria

Up to 124 Units of any solid oral benzodiazepines paid by Medicaid per
the previous 31 calendar days.
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Tenofovir (Viread)
(Implemented 12/19/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria



A billed diagnosis of HIV/AIDS in the Medicaid history in previous 2
years; OR
Paid drug claim(s) in Medicaid history of other antiretroviral therapy
(ART), such as non-nucleoside reverse transcriptase inhibitors
(NNRTI), OR protease inhibitors (PI), OR integrase strand transfer
inhibitor (INSTI) in previous 6 months.
A billed diagnosis of Hepatitis in the Medicaid history in previous 2
years.
Denial criteria


Therapeutic duplication edit: paid claim within previous 30 days for
Truvada; OR
Absence of approval criteria.
Approval criteria for PrEp will require a manual review PA process
based upon the following:





Documentation from prescriber that patient is at high risk for acquiring
HIV infection; AND
Negative HIV test before starting and every 3 months thereafter; AND
Pregnancy test before starting and every 3 months thereafter. If
pregnant, provide documentation of patient understanding of potential
risks and benefits of using Truvada®, including contraindication with
breastfeeding; AND
Serum creatinine lab tests obtained prior to initiation, then every 6
months. Creatinine clearance should be >60 mL/min; AND
Documented testing for Hepatitis B Virus (HBV) and results submitted.
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Tenofovir 300mg/Emtricitabine 200mg (Truvada)
(Implemented 12/19/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria for treatment of HIV-1 infection



A billed diagnosis of HIV/AIDS in the Medicaid history in previous 2
years; OR
Paid drug claim(s) in Medicaid history of other antiretroviral therapy
(ART), such as non-nucleoside reverse transcriptase inhibitors
(NNRTI), OR protease inhibitors (PI), OR integrase strand transfer
inhibitor (INSTI) in previous 6 months.
If there is no HIV/AIDS diagnosis in Medicaid history and no records of
other ART in the Medicaid drug profile, prescriber will be required to
follow the manual review process and submit documentation
confirming positive HIV diagnosis.
Denial criteria


Therapeutic duplication edit: paid claim within previous 30 days for
Emtriva® (emtricitabine) or Viread® (tenofovir disoproxil fumarate); OR
Absence of approval criteria.
Approval criteria for PrEp will require a manual review PA process
based upon the following:





Documentation from prescriber that patient is at high risk for acquiring
HIV infection; AND
Negative HIV test before starting and every 3 months thereafter; AND
Pregnancy test before starting and every 3 months thereafter. If
pregnant, provide documentation of patient understanding of potential
risks and benefits of using Truvada®, including contraindication with
breastfeeding; AND
Serum creatinine lab tests obtained prior to initiation, then every 6
months. Creatinine clearance should be >60 mL/min; AND
Documented testing for Hepatitis B Virus (HBV) and results submitted.
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Terbinafine 125mg and 187.5mg Granules Packet
(Lamisil)
(Implemented 04/12/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria


At least one paid claim in Medicaid history for fluconazole suspension in
the past 14-90 days, AND
At least 2 paid claims in Medicaid history for griseofulvin suspension in the
previous 14-90 days
AND
 No therapeutic duplication between two different strengths of Lamisil
granules.
Additional criteria

Quantity edits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Testosterone Replacement Products
(Implemented 01/18/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drug
Testosterone Cypionate 100 mg/ml Injection
Testosterone Cypionate 200 mg/ml Injection
Testosterone Enanthate 200 mg/ml Injection
Approval criteria


Male
Diagnosis of one of the following diagnoses in the previous 2 years:
o Hypospadias
o Klinefelter Syndrome
o Kallmann Syndrome
o Panhypopituitarism
o Prader-Willi Syndrome
Denial criteria


Female
Diagnosis of one of the following diagnoses in the previous 2 years:
o Decreased libido
o Impotence
o Any other sexual dysfunction diagnoses
Exceptions (Request through Manual Review Process)
Approve for women with diagnosis of breast cancer or hormone-responsive
tumor in history
Testosterone Products which require a Manual Review










Androderm 2 mg/24hr Patch
Androderm 4 mg/24hr Patch
Androgel 1% Gel
Android 10 mg Capsule
Androxy 10 mg Tablet
Aveed 750 mg/3 ml Vial
Axiron 30 mg Actuation Solution
Fortesta 10 mg Gel Pump
Methitest 10 mg Tablet
Striant 30 mg Mucoadhesive
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria


Testim 1% Gel
Testred Capsules
Additional Criteria

Quantity Limits Apply
Link to Memorandum
Link to Updated Criteria
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Tetrabenazine Tablet (Xenazine)
(Implemented 09/21/2009)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
Diagnosis of Huntington’s Disease with Chorea in the past 3 years.
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Timolol Maleate/Dorzolamide HCL (Cosopt PF)
(Implemented 07/09/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Cosopt PF
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Tiotropium Bromide Inhaler (Spiriva)
(Implemented 12/19/2012)
Prescribers may request an override for nonpreferred drugs by calling the
UAMS College of Pharmacy Evidence-Based Prescription Drug Program
Help Desk at 1-866-250-2518 (toll-free) or 501-526-4200 (local).
Approval criteria



Diagnosis of COPD in Medicaid history in previous 2 years; AND
No therapeutic duplication with overlapping days’ supply between
Anoro Ellipta, Spiriva, and/or Tudorza; AND
Medicaid recipient is > 18 years of age; AND
Denial criteria


Lack of approval criteria; OR
Diagnosis of asthma in Medicaid history in previous 2 years
Additional criteria

Quantity edits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Tobacco-cessation Products
(Implemented 11/15/2005)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
Bupropion (Zyban)
 Currently pregnant, OR
 < 60 days post partum, OR
 < 187 days of bupropion (Zyban) in the last 365 days.
Nicotine Replacement Therapy (Nicotine Gum and Patches)
 Currently pregnant, OR
 < 60 days post partum, OR
 < 187 days of nicotine replacement therapy in the last 365 days.
Varenicline (Chantix) Implemented 08/01/2007
 Currently pregnant, OR
 < 60 days post partum, OR
 < 187 days of varenicline in the last 365 days.
Denial criteria
Bupropion (Zyban)
 Therapeutic duplication of Chantix.
Nicotine Replacement Therapy (Gum and Patches)
 Therapeutic duplication of nicotine gum and nicotine patches.
 Therapeutic duplication of Chantix.
Varenicline (Chantix)
 Therapeutic duplication of nicotine gum
 Therapeutic duplication of nicotine patches
 Therapeutic duplication of Zyban
Link to Memorandum
Link to Memorandum for Chantix
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Tobramycin Inhalation Solution (TOBI – Brand Name)
(Implemented 01/09/2008)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
Diagnosis of cystic fibrosis in medical history
Denial criteria
History of Cayston in the past 50 days
History of J Code for Tobramycin Injection in the past 60 days
History of Bethkis in the past 50 days
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Tobramycin Inhalation Solution (Generic) (Bethkis)
(Implemented 03/18/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization


Generic Tobramycin Inhalation Solution
Bethkis
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Tobramycin Inhalation Powder (TOBI Podhaler)
(Implemented 12/10/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

TOBI Podhaler
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Topical Corticosteroids
(Implemented 03/26/2008)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria
A trial of at least two different products containing a different drug entity within
the same potency category that do not require prior authorization within the
previous 60 days. (Appendix C.)
TOPICAL CORTICOSTEROID PA LIST BY POTENCY
POTENCY
PA STATUS DRUG NAME
VERY HIGH
No PA
CLOBETASOL PROPIONATE 0.05% CREAM [TEMOVATE® CREAM]
VERY HIGH
No PA
CLOBETASOL PROPIONATE 0.05% EMOLLIENT CREAM [TEMOVATE
EMOLLIENT® CREAM]
VERY HIGH
No PA
CLOBETASOL PROPIONATE 0.05% GEL
VERY HIGH
No PA
CLOBETASOL PROPIONATE 0.05% OINTMENT [TEMOVATE® OINTMENT]
VERY HIGH
No PA
CLOBETASOL PROPIONATE 0.05% SOLUTION
VERY HIGH
No PA
HALOBETASOL PROPIONATE 0.05% CREAM [ULTRAVATE® CREAM]
VERY HIGH
No PA
HALOBETASOL PROPIONATE 0.05% OINTMENT [ULTRAVATE®
OINTMENT]
VERY HIGH
PA
BETAMETHASONE DIPROPIONATE AUGMENTED 0.05% OINTMENT
[DIPROLENE® OINTMENT]
VERY HIGH
PA
CLOBETASOL PROPIONATE 0.05% FOAM [OLUX® FOAM]
VERY HIGH
PA
CLOBETASOL PROPIONATE 0.05% EMOLLIENT FOAM [OLUX-E® FOAM]
VERY HIGH
PA
CLOBETASOL PROPIONATE 0.05% LOTION [CLOBEX® LOTION]
VERY HIGH
PA
CLOBETASOL PROPIONATE 0.05% SHAMPOO [CLOBEX® SHAMPOO]
VERY HIGH
PA
CLOBETASOL PROPIONATE 0.05% SPRAY [CLOBEX® SPRAY]
VERY HIGH
PA
DIFLORASONE DIACETATE 0.05% OINTMENT
VERY HIGH
PA
FLUOCINONIDE 0.01% CREAM [VANOS® CREAM]
Continued
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Approval criteria
A trial of at least two different products containing a different drug entity within
the same potency category that do not require prior authorization within the
previous 60 days. (Appendix C.)
POTENCY
PA STATUS DRUG NAME
HIGH
No PA
HIGH
No PA
HIGH
HIGH
HIGH
HIGH
HIGH
HIGH
HIGH
HIGH
HIGH
HIGH
HIGH
HIGH
HIGH
HIGH
HIGH
HIGH
HIGH
HIGH
HIGH
HIGH
No PA
No PA
No PA
No PA
No PA
No PA
No PA
No PA
No PA
No PA
No PA
PA
PA
PA
PA
PA
PA
PA
PA
PA
HIGH
PA
HIGH
HIGH
PA
PA
BETAMETHASONE DIPROPIONATE 0.05% CREAM
BETAMETHASONE DIPROPIONATE AUGMENTED 0.05% CREAM
[DIPROLENE AF® CREAM]
BETAMETHASONE DIPROPIONATE 0.05% LOTION
BETAMETHASONE VALERATE 0.1% OINTMENT
DESOXIMETASONE 0.25% CREAM [TOPICORT® CREAM]
DIFLORASONE DIACETATE 0.05% CREAM
FLUOCINONIDE 0.05% CREAM
FLUOCINONIDE 0.05% EMOLLIENT CREAM
FLUOCINONIDE 0.05% GEL
FLUOCINONIDE 0.05% OINTMENT
FLUOCINONIDE 0.05% SOLUTION
TRIAMCINOLONE ACETONIDE 0.5% CREAM
TRIAMCINOLONE ACETONIDE 0.5% OINTMENT
AMCINONIDE 0.1% CREAM
AMCINONIDE 0.1% LOTION
AMCINONIDE 0.1% OINTMENT
BETAMETHASONE DIPROPIONATE 0.05% OINTMENT
DESOXIMETASONE 0.05% CREAM [TOPICORT® CREAM]
DESOXIMETASONE 0.05% GEL [TOPICORT® GEL]
DESOXIMETASONE 0.05% OINTMENT [TOPICORT® OINTMENT]
DESOXIMETASONE 0.25% OINTMENT [TOPICORT® OINTMENT]
DESOXIMETASONE 0.25% SPRAY [TOPICORT® SPRAY]
DIFLORASONE DIACETATE 0.05% EMOLLIENT CREAM [APEXICON® E
CREAM]
HALCINONIDE 0.1% CREAM [HALOG® CREAM]
HALCINONIDE 0.1% OINTMENT [HALOG® OINTMENT]
Continued
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Approval criteria
A trial of at least two different products containing a different drug entity within
the same potency category that do not require prior authorization within the
previous 60 days. (Appendix C.)
POTENCY
PA STATUS DRUG NAME
MEDIUM
MEDIUM
MEDIUM
MEDIUM
MEDIUM
MEDIUM
MEDIUM
MEDIUM
MEDIUM
MEDIUM
MEDIUM
MEDIUM
MEDIUM
MEDIUM
MEDIUM
MEDIUM
MEDIUM
MEDIUM
No PA
No PA
No PA
No PA
No PA
No PA
No PA
No PA
No PA
No PA
No PA
No PA
No PA
No PA
No PA
No PA
No PA
PA
MEDIUM
PA
MEDIUM
MEDIUM
MEDIUM
PA
PA
PA
MEDIUM
PA
MEDIUM
MEDIUM
PA
PA
MEDIUM
PA
MEDIUM
MEDIUM
MEDIUM
MEDIUM
PA
PA
PA
PA
MEDIUM
PA
MEDIUM
PA
BETAMETHASONE VALERATE 0.1% CREAM
BETAMETHASONE VALERATE 0.1% LOTION
FLUTICASONE PROPIONATE 0.005% OINTMENT
FLUTICASONE PROPIONATE 0.05% CREAM
HYDROCORTISONE BUTYRATE 0.1% CREAM
HYDROCORTISONE BUTYRATE 0.1% OINTMENT
HYDROCORTISONE BUTYRATE 0.1% SOLUTION
HYDROCORTISONE VALERATE 0.2% CREAM
MOMETASONE FUROATE 0.1% CREAM [ELOCON® CREAM]
MOMETASONE FUROATE 0.1% OINTMENT [ELOCON® OINTMENT]
MOMETASONE FUROATE 0.1% SOLUTION [ELOCON® SOLUTION]
TRIAMCINOLONE ACETONIDE 0.025% CREAM
TRIAMCINOLONE ACETONIDE 0.025% LOTION
TRIAMCINOLONE ACETONIDE 0.025% OINTMENT
TRIAMCINOLONE ACETONIDE 0.1% CREAM
TRIAMCINOLONE ACETONIDE 0.1% LOTION
TRIAMCINOLONE ACETONIDE 0.1% OINTMENT
BETAMETHASONE DIPROPIONATE AUGMENTED 0.05% GEL
BETAMETHASONE DIPROPIONATE AUGMENTED 0.05% LOTION
[DIPROLENE® LOTION]
BETAMETHASONE VALERATE 0.12% FOAM [LUXIQ® FOAM]
CLOCORTOLONE PIVALATE 0.1% CREAM [CLODERM® CREAM]
FLUOCINOLONE ACETONIDE 0.025% CREAM [SYNALAR® CREAM]
FLUOCINOLONE ACETONIDE 0.025% OINTMENT [SYNALAR ®
OINTMENT]
FLURANDRENOLIDE 4 MCG/SQ CM TAPE [CORDRAN® TAPE]
FLUTICASONE PROPIONATE 0.05% LOTION [CUTIVATE® LOTION]
HYDROCORTISONE BUTYRATE 0.1% EMOLLIENT CREAM [LOCOID®
LIPOCREAM]
HYDDROCORTISONE PROBUTATE 0.1% CREAM [PANDEL® CREAM]
HYDROCORTISONE VALERATE 0.2% OINTMENT
PREDNICARBATE 0.1% CREAM [DERMATOP® CREAM]
PREDNICARBATE 0.1% OINTMENT [DERMATOP® OINTMENT]
TRIAMCINOLONE ACETONIDE 0.147 MG/GM AEROSOL SPRAY
[KENALOG® SPRAY]
TRIAMCINOLONE ACETONIDE 0.05% OINTMENT [TRIANEX® OINTMENT]
Continued
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Approval criteria
A trial of at least two different products containing a different drug entity within
the same potency category that do not require prior authorization within the
previous 60 days. (Appendix C.)
POTENCY
PA STATUS
LOW
No PA
LOW
LOW
No PA
No PA
LOW
No PA
LOW
LOW
LOW
LOW
LOW
LOW
LOW
LOW
LOW
LOW
LOW
LOW
LOW
No PA
No PA
No PA
No PA
No PA
No PA
No PA
No PA
PA
PA
PA
PA
PA
LOW
PA
LOW
PA
LOW
PA
DRUG NAME
ALCLOMETASONE DIPROPIONATE 0.05% CREAM
ALCLOMETASONE DIPROPIONATE 0.05% OINTMENT
DESONIDE 0.05% OINTMENT
FLUOCINOLONE ACETONIDE 0.01% OIL [DERMA-SMOOTHE
FS®]
HYDROCORTISONE 0.5% CREAM
HYDROCORTISONE 0.5% OINTMENT
HYDROCORTISONE 1% CREAM
HYDROCORTISONE 1% OINTMENT
HYDROCORTISONE 2.5% CREAM
HYDROCORTISONE 2.5% LOTION
HYDROCORTISONE 2.5% OINTMENT
HYDROCORTISONE ACETATE 0.5% CREAM
DESONIDE 0.05% CREAM
DESONIDE 0.05% FOAM [VERDESO® FOAM]
DESONIDE 0.05% GEL [DESONATE® GEL]
DESONIDE 0.05% LOT (DESOWEN ®)
FLUOCINOLONE ACETONIDE 0.01% CREAM
FLUOCINOLONE ACETONIDE 0.01% SHAMPOO [CAPEX®
SHAMPOO]
FLUOCINOLONE ACETONIDE 0.01% SOLUTION [SYNALAR®
SOLUTION]
HYDROCORTISONE 2.5% SOLUTION [TEXACORT® SOLUTION]
Denial criteria
Failure to meet approval criteria
Link to Memorandum
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Topical Products
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require a manual PA
Altabax 1% ointment
Implemented 09/21/2009
o
Generic mupirocin is available without prior authorization
Bensal® HP (benzoic acid 6%, salicylic Acid 3%, Oak Bark Extract)
Ointment
Implemented April 6, 2010
Nucort lotion (hydrocortisone acetate-aloe vera)
Implemented 01/12/2010
o
o
Generic hydrocortisone is available without prior authorization
Nuzon gel (hydrocortisone acetate-aloe vera)
Implemented 01/12/2010
o
o
Generic hydrocortisone is available without prior authorization
Ulesfia 5% lotion
Implemented 01/12/2010
o
Permethrin products are available without prior authorization
Link to Memorandum Ulesfia
Link to Memorandum Bensal HP
Link to Memorandum Altabax
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Topiramate XR Capsules (Qudexy XR and Trokendi
XR)
(Implemented 12/10/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization


Qudexy XR
Trokendi XR
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Tramadol Extended-Release (Conzip Capsule and
Ryzolt ER Tablet)
(Implemented 01/12/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that do not require manual review for prior authorization

Tramadol ER (Ultram ER)
Drugs that require manual review for prior authorization


Conzip capsule
Ryzolt ER tablet
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Tramadol Immediate-Release (Ultram, Ultracet)
(Implemented 04/21/2009)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria



Diagnosis of cancer in the past 12 months, AND
No claim in history for Subutex, AND
No claim in history for Suboxone.



Paid claim for an antineoplastic in the past 12 months, AND
No claim in history for Subutex, AND
No claim in history for Suboxone.

Therapeutic duplication between short-acting opioids with less than 25%
of the days’ supply remaining on the previous claim, OR
Therapeutic duplication between a short-acting opioid and tramadol IR
(Ultram) with less than 25% of the days’ supply remaining on the previous
claim, OR
Therapeutic duplication between a short-acting opioid and
tramadol/acetaminophen (Ultracet) with less than 25% of the days’ supply
remaining on the previous claim.
Therapeutic duplication between a tramadol IR and
tramadol/acetaminophen (Ultracet) with less than 25% of the days’ supply
remaining on the previous claim.
Therapeutic duplication between a short-acting opioid and tramadol ODT
(Rybix) with less than 25% of the days’ supply remaining on the previous
claim.




Denial criteria
Paid Medicaid claim for Suboxone or Subutex in the past 60 days
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Trametinib (Mekinist) Tablets
(Implemented 09/18/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Mekinist
Additional Criteria

Quantity Limits Apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Tranexamic Acid (Lysteda)
(Implemented 06/21/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Lysteda
Additional criteria
Quantity limits apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Transdermal Scopolamine Patches
(Implemented 03/09/2010)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria


≥ 12 years of age, OR
History of at least one paid claim in the past 60 days for transderm
scopolamine
Additional criteria
Quantity limits apply
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Trazodone HCL (Oleptro ER 150mg & 300mg,
Trazodone 300mg) Tablet
(Implemented 07/09/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization


Oleptro ER 150mg, 300mg tablet
Trazodone 300mg tablet
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Trientine HCl (Syprine) Capsule
(Implemented 09/18/2013)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Syprine
Additional Criteria

Quantity Limits Apply
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Uloric Tablet (Febuxostat)
(Implemented 08/17/2010)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that do not require prior authorization

Allopurinol tablets
Drugs that require manual review for prior authorization

Uloric tablet
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Umeclidinium-Vilanterol Inhalation Powder (Anoro
Ellipta)
Prescribers may request an override for nonpreferred drugs by calling the
UAMS College of Pharmacy Evidence-Based Prescription Drug Program
Help Desk at 1-866-250-2518 (toll-free) or 501-526-4200 (local).
Approval criteria



Diagnosis of COPD in Medicaid history in previous 2 years; AND
No therapeutic duplication with overlapping days’ supply between
Anoro Ellipta, Spiriva, and/or Tudorza; AND
Medicaid recipient is > 18 years of age; AND
Denial criteria


Lack of approval criteria; OR
Diagnosis of asthma in Medicaid history in previous 2 years
Additional criteria

Quantity edits apply
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Valganciclovir Oral Solution (Valcyte)
(Implemented 01/18/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Approval criteria


Less than 9 years of age, OR
History of diagnosis of NPO in Medicaid History
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Vemurafenib Tablet (Zelboraf)
(Implemented 04/17//2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Zelboraf tablet
Information required for the manual review process
 Confirmation of BRAFV600E mutation-positive melanoma as detected by an
FDA-approved test
 In addition to requirement of diagnosis and lab results showing BRAFV600E
mutation-positive melanoma, the following data will be required for the manual
review process:
o Baseline EKG and then every 3 months thereafter to monitor for QTc
o Liver function tests baseline and then periodic
o Baseline and periodic dermatology evaluation for squamous cell
carcinomas
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Vismodegib Capsule (Erivedge)
(Implemented 07/09/2012)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Erivedge capsule
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Vorapaxar (Zontivity)
(Implemented 09/23/2014)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Zontivity
Link to Memorandum
Top of the document
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Xgeva (Denosumab)
(Implemented 01/21/2011)
Prescribers may request an override by calling the HP Help Desk at 1-800707-3854 (toll-free) or 501-374-6609 ext. 500 (local).
Drugs that require manual review for prior authorization

Xgeva
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Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Xolair
(Implemented 08/01/2003)
Prescribers are required to fax a letter of medical necessity and include all
supporting documentation for manual review to 501-683-4124.
Link to Xolair statement of necessity—Microsoft Word format (.doc):
https://www.medicaid.state.ar.us/Download/provider/forms/pharm/xolair.doc
Link to Xolair statement of necessity—Portable Document Format (.pdf):
https://www.medicaid.state.ar.us/Download/provider/forms/pharm/xolair.pdf
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Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Appendix A – Nil per os (NPO)
ICD-9/Procedure codes
B4034, B4035, B4036
B4149, B4150-B4156
B4160-B4162
43.11
46.32
96.07
97.01
432.46
432.60
437.52
437.6
437.61
438.3
438.32
440.15
443.72
443.73
494.4
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Description
Enteral feeding supplies
Enteral formula
Enteral formula for pediatrics
PEG
PEJ tube
Nasogastric tube insertion
Nasogastric tube placement
PEG placement
PEG placement
Naso/Oro-gastric tube placement
Gastrostomy tube
G-tube repositioning
Gastrostomy tube
Gastrostomy tube
J-Tube
J-Tube
J-Tube
PEG placement
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Appendix B – Approved tracheostomy codes
Code
V44.0
V55.0
31.1
31.2X
31.74
519.0X
31600
31601
31603
31605
31610
Description
Tracheostomy status
Attention to tracheostomy
Temporary tracheostomy
Permanent tracheostomy
Revision of tracheostomy
Tracheostomy complications
Tracheostomy, planned (separate procedure);
Tracheostomy, planned (separate procedure); younger than two
years
Tracheostomy, emergency procedure; transtracheal
Tracheostomy, emergency procedure; cricothyroid membrane
Tracheostomy, fenestration procedure with skin flaps
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Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Appendix C – Topical corticosteroids, no PA required
Very high potency – No PA required
POTENCY
Very high
PA STATUS
Very high
No PA
Very high
No PA
CLOBETASOL PROPIONATE 0.05% GEL
Very high
No PA
CLOBETASOL PROPIONATE 0.05% OINTMENT [TEMOVATE®
OINTMENT]
Very high
No PA
CLOBETASOL PROPIONATE 0.05% SOLUTION
Very high
No PA
HALOBETASOL PROPIONATE 0.05% CREAM [ULTRAVATE®]
Very high
No PA
HALOBETASOL PROPIONATE 0.05% OINTMENT
[ULTRAVATE® OINTMENT]
No PA
DRUG NAME
CLOBETASOL PROPIONATE 0.05% CREAM [tEMOVATE ®
CREAM)
CLOBETASOL PROPIONATE 0.05% EMOLLIENT CREAM
[TEMOVATE EMOLLIENT® CREAM]
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Topical Corticosteroid Criteria
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
High potency – No PA required
POTENCY
PA STATUS
DRUG NAME
High
No PA
BETAMETHASONE DIPROPIONATE 0.05% CREAM
High
No PA
BETAMETHASONE DIPROPIONATE AUGMENTED 0.05%
CREAM [DIPROLENE AF® CREAM]
High
No PA
BETAMETHASONE DIPROPIONATE 0.05% LOTION
High
No PA
BETAMETHASONE VALERATE 0.1% OINTMENT
High
No PA
DESOXIMETASONE 0.25% CREAM [TOPICORT® CREAM]
High
No PA
DIFLORASONE DIACETATE 0.05% CREAM
High
No PA
FLUOCINONIDE 0.05% CREAM
High
No PA
FLUOCINONIDE 0.05% EMOLLIENT CREAM
High
No PA
FLUOCINONIDE 0.05% GEL
High
No PA
FLUOCINONIDE 0.05% OINTMENT
High
No PA
FLUOCINONIDE 0.05% SOLUTION
High
No PA
TRIAMCINOLONE ACETONIDE 0.5% CREAM
High
No PA
TRIAMCINOLONE ACETONIDE 0.5% OINTMENT
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Topical Corticosteroid Criteria
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Medium potency – No PA required
POTENCY
PA STATUS
DRUG NAME
Medium
No PA
BETAMETHASONE VALERATE 0.1% CREAM
Medium
No PA
BETAMETHASONE VALERATE 0.1% LOTION
Medium
No PA
FLUTICASONE PROPIONATE 0.005% OINTMENT
Medium
No PA
Medium
No PA
FLUTICASONE PROPIONATE 0.05% CREAM
HYDROCORTISONE BUTYRATE 0.1% CREAM
Medium
No PA
HYDROCORTISONE BUTYRATE 0.1% OINTMENT
Medium
No PA
HYDROCORTISONE BUTYRATE 0.1% SOLUTION
Medium
No PA
HYDROCORTISONE VALERATE 0.2% CREAM
Medium
No PA
MOMETASONE FUROATE 0.1% CREAM
Medium
No PA
MOMETASONE FUROATE 0.1% OINTMENT
Medium
No PA
MOMETASONE FUROATE 0.1% SOLUTION
Medium
No PA
TRIAMCINOLONE ACETONIDE 0.025% CREAM
Medium
No PA
TRIAMCINOLONE ACETONIDE 0.025% LOTION
Medium
No PA
TRIAMCINOLONE ACETONIDE 0.025% OINTMENT
Medium
No PA
TRIAMCINOLONE ACETONIDE 0.1% CREAM
Medium
No PA
TRIAMCINOLONE ACETONIDE 0.1% LOTION
Medium
No PA
TRIAMCINOLONE ACETONIDE 0.1% OINTMENT
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Topical Corticosteroid Criteria
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Low potency – No PA required
POTENCY
PA STATUS
DRUG NAME
Low
No PA
ALCLOMETASONE DIPROPIONATE 0.05% CREAM
Low
No PA
ALCLOMETASONE DIPROPIONATE 0.05% OINTMENT
Low
No PA
Low
No PA
Low
No PA
DESONIDE 0.05% OINTMENT
FLUOCINOLONE ACETONIDE 0.01% OIL (DERMA-SMOOTHE
FS®)
HYDROCORTISONE 0.5% CREAM
Low
No PA
HYDROCORTISONE 0.5% OINTMENT
Low
No PA
HYDROCORTISONE 1% CREAM
Low
No PA
HYDROCORTISONE 1% OINTMENT
Low
No PA
HYDROCORTISONE 2.5% CREAM
Low
No PA
HYDROCORTISONE 2.5% LOTION
Low
No PA
HYDROCORTISONE 2.5% OINTMENT
Low
No PA
HYDROCORTISONE ACETATE 0.5% CREAM
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Topical Corticosteroid Criteria
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Appendix D – Congestive heart failure diagnoses
ICD-9
402.01
402.11
402.91
404.01
404.03
404.11
404.13
404.91
404.92
404.93
428
Description
Hypertensive heart disease with heart failure
Hypertensive heart disease with heart failure
Hypertensive heart disease with heart failure
Hypertensive heart and renal disease with heart failure
Hypertensive heart and renal disease with heart and renal failure
Hypertensive heart and renal disease with heart failure
Hypertensive heart and renal disease with heart and renal failure
Hypertensive heart and renal disease with heart failure
Hypertensive heart and renal disease with renal failure
Hypertensive heart and renal disease with heart and renal failure
Congestive heart failure, unspecified
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Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Appendix E – Malignant cancer diagnoses
ICD-9
140
142
146
147
148
149
150
151
152
153
154
155
156
157
158
159
160
161
162
163
164
165
170
171
172
174
175
176
179
180
181
182
183
184
185
186
187
Description
Malignant neoplasm of lip
Malignant neoplasm of major salivary gland
Malignant neoplasm of oropharynx
Malignant neoplasm of nasopharynx
Malignant neoplasm of hypopharynx
Malignant neoplasm of other and ill-defined sites within the lip, oral
cavity, and pharynx
Malignant neoplasm of esophagus
Malignant neoplasm of stomach
Malignant neoplasm of small intestine including duodenum
Malignant neoplasm of colon
Malignant neoplasm of rectum rectosigmoid junction
Malignant neoplasm of liver and intrahep
Malignant neoplasm of gall bladder and extrahepatic bile duct
Malignant neoplasm of pancreas
Malignant neoplasm of retroperitoneum and peritoneum
Malignant neoplasm of other and ill-defined sites within the digestive
organs and peritoneum
Malignant neoplasm of nasal cavities middle ear and accessory sinuses
Malignant neoplasm of larynx
Malignant neoplasm of trachea bronchus and lung
Malignant neoplasm of pleura
Malignant neoplasm of thymus, heart, and mediastinum
Malignant neoplasm of other and ill-defined sites within the respiratory
system and intrathoracic organs
Malignant neoplasm of bone and articular cartilage
Malignant neoplasm of connective and other soft tissue
Malignant melanoma of skin
Malignant neoplasm of female breast
Malignant neoplasm of male breast
Kaposis sarcoma
Malignant neoplasm of uterus, part unspecified
Malignant neoplasm of cervix uteri
Malignant neoplasm of placenta
Malignant neoplasm of body of uterus
Malignant neoplasm of ovary and other uterine adnexa
Malignant neoplasm other and unspecified female genital organs
Malignant neoplasm of prostate
Malignant neoplasm of testis
Malignant neoplasm of penis and other male genital
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
ICD-9
188
189
190
191
192
193
194
195
196
197
198
199
200
201
202
203
204
205
206
207
208
Description
Malignant neoplasm of bladder
Malignant neoplasm of kidney and other and unspecified urinary organs
Malignant neoplasm of eye
Malignant neoplasm of brain
Malignant neoplasm other and unspecified parts nervous system
Malignant neoplasm of thyroid gland
Malignant neoplasm of other endocrine glands and related structures
Malignant neoplasm of other and ill-defined sites
Secondary and unspecified malignant neoplasm of lymph
Secondary malignant neoplasm of respiratory and digestive
Secondary malignant neoplasm of other specified sites
Malignant neoplasm without specification
Lymphosarcoma and reticulosarcoma
Hodgkins disease
Other malignant neoplasms lymphoid and histiocytic tissue
Multiple myeloma and immunoproliferative neoplasms
Lymphoid leukemia
Myeloid leukemia
Monocytic leukemia
Other specified leukemia
Leukemia of unspecified cell type
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Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Appendix F – Antineoplastics to infer malignant
cancer
Antineoplastics
Aldesleukin
Alemtuzumab
Altretamine
Amifostine
Arsenic
Asparaginase
Bcg
Bevacizumab
Bleomycin
Busulfan
Capecitabine
Carboplatin
Carmustine
Cisplatin
Clofarabine
Cytarabine
Dacarbazine
Dactinomycin
Daunorubicin
Denileukin
Docetaxel
Doxorubicin
Estramustine
Etoposide
Exemestane
Floxuridine
Fludarabine
Fluorouracil
Fulvestrant
Gefitinib
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Gemcitabine
Gemtuzumab
Idarubicin
Ifosfamide
Ifosfamide/mesna
Imatinib
Lomustine
Mechlorethamine
Mitomycin
Mitoxantrone
Oxaliplatin
Paclitaxel
Paclitaxel,semi-synthetic
Pegaspargase
Pemetrexed
Pentostatin
Plicamycin
Procarbazine
Rasburicase
Rituximab
Streptozocin
Temozolomide
Teniposide
Thiotepa
Topotecan
Trastuzumab
Vinblastine
Vincristine
Vinorelbine
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Appendix G – Chronic obstruction pulmonary disease
diagnoses
ICD-9
492
496
Description
Emphysema
Chronic airway obstruction, not elsewhere classified
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Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Appendix H – Approved diagnoses for nonpreferred
antiepileptic agents in neuropathic pain agent class
ICD-9
46.2
54.3
238.7
253.5
291.81
292
293.81
Description
Subacute sclerosing panencephalitis
Herpes simplex meningoencephalitis
Other lymphatic and hematopoietic tissues
Diabetes insipidus
Alcohol withdrawal
Drug withdrawal syndrome
Psychotic disorder with delusions in conditions classified elsewhere
Psychotic disorder with hallucinations in conditions classified
293.82
elsewhere
294.1XX Dementia in conditions classified elsewhere
295.XX Schizophrenic disorders
296.XX Affective psychoses (manic, depressive, bi-polar)
Psychoses with origin specific to childhood (pervasive developmental
299.XX disorders)
300.01
Panic disorder
300.23
Social phobia
300.3
Obsessive compulsive disorder
300.4
Neurotic depression
301.12
Chronic depressive personality disorder
301.2
Schizoid personality disorder
301.4
Obsessive compulsive disorder
301.83
Borderline personality disorder
304.2
Cocaine dependence
306.1
Physiological malfunction arising from mental factors, respiratory
307.2X
Tics
307.81
Tension headache
308.2
Predominant psychomotor disturbance
309.XX Adjustment reaction
Unspecified nonpsychotic mental disorder following organic brain
310.9
damage
311
Depressive disorder
312.X
Disturbance of conduct
313.XX Disturbance of emotions specific to childhood adolescence
317.XX Mild mental retardation
318.XX Other specified mental retardation
319.XX Unspecified mental retardation
327.51
Periodic limb movement disorder
330.1
Cerebral lipidoses
330.8
Rett’s disorder
Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
ICD-9
Description
332.XX Parkinson’s disease
333.XX Other extrapyramidal disease and abnormal movement disorder
340
Multiple sclerosis
345.XX Epilepsy
346.XX Migraine
353.6
Phantom limb syndrome
359.2
Myotonic disorder
368.16
Psychophysical visual disturbance
388.3X
Tinnitis
392.XX Rheumatic chorea
438.81
Apraxia
588.1
Nephrogenic diabetes insipidus
625.4
Premenstrual tension syndromes
696.1
Erythrodermic psoriasis
759.81
Prader-willi syndrome
759.89
Angelman syndrome
779.XX Other and ill defined conditions originating in the perinatal period
780.3X
Convulsions, seizures
781.XX Abnormal involuntary movements
784.69
Symbolic dysfunction, unspecified, other
786.8
Hiccough
854.XX Intracranial injury
V11.0
Schizophrenia
V11.1
Affective disorders
V11.3
Alcoholism
V17.2
Other neurological diseases
V18.4
Mental retardation
V79.0
Depression
V79.2
Mental retardation
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Arkansas Medicaid Prescription Drug Program Prior Authorization Criteria
Appendix I – Approved endoscopy codes
Endoscopy
CPT
43201
43234
43235
43236
43237
43238
43239
43240
43241
43242
43243
43244
43245
43246
43247
43248
43249
43250
43251
43255
43256
43257
43258
43259
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Procedure
ESPHGSC RGD/FLX DIRED SBMCSL NJX ANY SBST
UPR GI NDSC SMPL PRIM XM SPX
UPR GI NDSC DX +-COLLJ SPEC BR/WA SPX
UPR GI NDSC DIRED SBMCSL NJX ANY SBST
UPR GI NDSC NDSC US XM LMTD ESOPH
UPR GI NDSC TNDSC US FINE NDL ASPIR/BX ESOPH
UPR GI NDSC BX 1/MLT
UPR GI NDSC TRANSMURAL DRG PSEUDOCST
UPR GI NDSC TNDSC INTRAL TUBE/CATH PLMT
UPR GI NDSC TNDSC US FINE NDL ASPIR/BX W/US XM
UPR GI NDSC NJX SCLEROSIS ESOPHGL&/GSTR VARC
UPR GI NDSC BAND LIG ESOPHGL&/GSTR VARC
UPR GI NDSC DILAT GSTR OUTLET FOR OBSTRCJ
UPR GI NDSC DIRED PLMT PRQ GASTROSTOMY TUBE
UPR GI NDSC RMVL FB
UPR GI NDSC INSJ GD WIRE DILAT ESOPH GD WIRE
UPR GI NDSC BALO DILAT ESOPH <30 MM DIAM
UPR GI NDSC RMVL LES HOT BX/BIPOLAR CAUT
UPR GI NDSC RMVL TUM POLYP/OTH LES SNARE TQ
UPR GI NDSC CTRL BLD ANY METH
UPR GI NDSC TNDSC STENT PLMT W/PREDILAT
UPR GI NDSC DLVR THERMAL NRG SPHNCTR/CARDIA
UPR GI NDSC ABLTJ LES X RMVL FORCEPS/CAUT/SNARE
UPR GI NDSC W/US XM